JPH07110326B2 - ▲ Ro ▼ over filter - Google Patents
▲ Ro ▼ over filterInfo
- Publication number
- JPH07110326B2 JPH07110326B2 JP2310488A JP2310488A JPH07110326B2 JP H07110326 B2 JPH07110326 B2 JP H07110326B2 JP 2310488 A JP2310488 A JP 2310488A JP 2310488 A JP2310488 A JP 2310488A JP H07110326 B2 JPH07110326 B2 JP H07110326B2
- Authority
- JP
- Japan
- Prior art keywords
- zinc
- zinc oxide
- filter
- water
- firing
- 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 - Lifetime
Links
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 26
- 239000011787 zinc oxide Substances 0.000 claims description 13
- 239000011521 glass Substances 0.000 claims description 9
- 238000010304 firing Methods 0.000 claims description 8
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 229910052725 zinc Inorganic materials 0.000 description 8
- 239000011701 zinc Substances 0.000 description 8
- 239000011148 porous material Substances 0.000 description 7
- 239000000843 powder Substances 0.000 description 7
- 239000013078 crystal Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- 230000035699 permeability Effects 0.000 description 6
- 239000011230 binding agent Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- -1 wire mesh Substances 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 238000000498 ball milling Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000007596 consolidation process Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000013505 freshwater Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000012784 inorganic fiber Substances 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 238000002161 passivation Methods 0.000 description 1
- 238000005554 pickling Methods 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
Landscapes
- Filtering Materials (AREA)
- Porous Artificial Stone Or Porous Ceramic Products (AREA)
Description
【発明の詳細な説明】 産業上の利用分野 本発明は汚れ処理,造水等の水処理フィルター,空気浄
化フィルター,食品工業等の懸濁液処理フィルター,化
学工業等の水,排水プロセス・フィルター等として利用
される過フィルターに関する。TECHNICAL FIELD The present invention relates to a water treatment filter for soil treatment, fresh water, etc., an air purifying filter, a suspension treatment filter for the food industry, water for the chemical industry, drainage process filter. For overfilters used as
従来の技術 従来の過フィルターには、紙,布等の有機質繊
維をからませて連結したもの、不織布のように別種バイ
ンダーで連結したもの、金網,ガラスマット,ガラス
クロスの如く細線物,無機質繊維を互に絡せたり、バイ
ンダーで連結したもの、有機シート状物に網孔、微細
孔を発現させたもの、焼結金属のように無機非繊維質
粒状物を溶着又は別種バインダーで連結したもの等があ
る。Conventional technology Conventional overfilters are made by entwining organic fibers such as paper, cloth, etc., connected by another kind of binder such as non-woven fabric, wire mesh, glass mat, glass cloth, fine wire, inorganic fiber. Entangled with each other or connected with a binder, organic sheet-like material with network pores and fine pores developed, inorganic non-fibrous granular material such as sintered metal welded or connected with another kind of binder Etc.
発明が解決しようとする課題 これらはそれぞれな特長を有するが、過効率の点で
は、は繊維状物の径が小ならば低圧下では拒絶性,
透過性共に良好であるが、高圧下では繊維部分の変形に
より圧密化して透過性が低下する。では低圧下でも孔
形成密度に限界があり透過性が前者より劣る。又高圧下
では圧密化により孔寸法が変化して透過率が下がる。
は低圧下,高圧下で孔寸法は変化しないが、空孔率が充
分に上がらない。Problems to be Solved by the Invention These have their respective characteristics, but in terms of over-efficiency, if the diameter of the fibrous material is small,
The permeability is good, but under high pressure, the fiber part is deformed to be consolidated and the permeability is lowered. However, even at low pressure, the pore formation density is limited and the permeability is inferior to the former. Also, under high pressure, the pore size changes due to consolidation, and the transmittance decreases.
The pore size does not change under low pressure and high pressure, but the porosity does not increase sufficiently.
本発明では従来の各種フィルターの問題点である高圧下
での過特性の低下を改良して、常圧下,高圧下共に高
拒絶率,高透過性を達成する過フィルターを提供しよ
うとするものである。The present invention is intended to provide an overfilter that achieves a high rejection rate and a high permeability both under normal pressure and under high pressure by improving the deterioration of overcharacteristics under high pressure, which is a problem of various conventional filters. is there.
課題を解決するための手段 本発明は2方向以上に分岐した構造を有する酸化亜鉛ウ
ィスカーにガラスフリットを添加し焼成してなるもので
ある。Means for Solving the Problems The present invention is one in which a glass frit is added to a zinc oxide whisker having a structure branched in two or more directions, followed by firing.
作 用 上記ウィスカーの針状部は互に絡り、細孔で且つ空孔率
の高い極めて秀れた材構造が達成される。孔径寸法は
成型時のプレス圧により縮り、針状部の交点は添加した
ガラスフリットの溶融により連結される。又、上記ウィ
スカーは水、溶媒等のぬれ特性が良好であり、単結晶で
内部格子欠かんの無い完全結晶強度に近似した強度を有
する素材であり高圧下でも全く変化なく、過特性を発
揮するものである。Working The needle-shaped portions of the above whiskers are entangled with each other, and an extremely excellent material structure having pores and high porosity is achieved. The pore size is reduced by the pressing pressure during molding, and the intersections of the needle-shaped parts are connected by melting the added glass frit. Further, the above whiskers have good wettability with water, solvent, etc., and are a single crystal material having a strength close to a perfect crystal strength with no internal lattice defect, and exhibit no excessive changes even under high pressure and exhibit over-characteristics. It is a thing.
実施例 以下、本発明の実施例について説明する。Examples Examples of the present invention will be described below.
まず、金属亜鉛を酸化して製造された酸化亜鉛ウィスカ
ーを準備する。具体的に説明すると、この酸化亜鉛ウィ
スカーは、従来の酸化亜鉛の製造方法や酸化亜鉛ウィス
カーの製造方法と異なり、金属亜鉛粉末を使用すること
によって得られる。それらの粒子径は0.1〜500μmが使
用可能であり、なかでも10〜300μmのものが最良の結
果となる。又これらの金属亜鉛粉末は亜鉛線や亜鉛粉末
をアーク式の溶射装置で空気中に溶射することにより得
た粉末が好ましいが、他の粉砕法,噴霧法,スタンプミ
ル法,ボールミル法より得られる上記範囲の亜鉛粉末を
用いることもできる。First, a zinc oxide whisker manufactured by oxidizing metallic zinc is prepared. More specifically, this zinc oxide whisker is obtained by using metallic zinc powder, which is different from the conventional methods for producing zinc oxide and zinc oxide whiskers. A particle size of 0.1 to 500 μm can be used, and a particle size of 10 to 300 μm gives the best result. Further, these metallic zinc powders are preferably powders obtained by spraying zinc wires or zinc powders into the air with an arc-type spraying device, but they can be obtained by other pulverizing methods, atomizing methods, stamp mill methods, ball mill methods. Zinc powder in the above range can also be used.
上記の亜鉛粉末の表面に酸化皮膜を形成する方法として
は、以下の方法が好ましい。まず、水共存下での機械的
処理として、乳針式擂漬機,ロール等で処理を行い、粒
子に機械的に圧力を加える。更にこれを水中に24時間以
上、なかでも76時間ならば如何なる大きさの粒子の粒子
径でも完全なる結果を与える。又放置温度は20℃以上に
保つことが好ましい。次に放置後乾燥する。この乾燥は
粉末表面の水切りが達成されればよく、次の焼成工程の
高温中へ移行した当初の幣害が防がれるように、即ちる
つぼ,割れ,粉のとび散りがなくなる程度に乾燥すれば
良好である。このため風乾から亜鉛粉末の溶融しない温
度範囲まで行うことができる。次に乾した粉末は耐熱容
器通常はアルミナ等のるつぼに入れ、酸素を含む雰囲気
中で600〜1500℃、なかでも900〜1100℃で加熱するのが
いかなる粒子径でも良好な結果を与える。As a method for forming an oxide film on the surface of the zinc powder, the following method is preferable. First, as mechanical treatment in the coexistence of water, treatment is carried out with a milk needle type pickling machine, rolls, etc., and mechanical pressure is applied to the particles. Furthermore, it gives complete results in particles of any size for more than 24 hours, especially 76 hours. Further, the standing temperature is preferably maintained at 20 ° C or higher. Next, it is left to dry. This drying only needs to be carried out so that the surface of the powder can be drained, and the drying should be carried out so as to prevent the initial damage caused by shifting to high temperature in the next firing step, that is, to the extent that crucibles, cracks, and scattering of powder do not occur. If it is good. For this reason, it is possible to perform from air drying to a temperature range where the zinc powder is not melted. The dried powder is then placed in a heat-resistant container, usually a crucible such as alumina, and heated in an atmosphere containing oxygen at 600 to 1500 ° C, especially 900 to 1100 ° C, to give good results with any particle size.
前記の加熱焼成は、通常空気中で行えばよいが、窒素と
酸素の混合ガス中で行ってもよい。The above heating and firing may be normally performed in air, but may be performed in a mixed gas of nitrogen and oxygen.
金属亜鉛粉末を、前記のように、水共存下で擂漬やロー
ル等で機械的圧力を付与することにより表面に酸化皮膜
が形成されるが、後の水中での放置によりこの皮膜が成
長する。これはX線回折法により確認された。又このよ
うにして形成した酸化皮膜は、特別な効果を与える。す
なわち乾燥雰囲気中で通常亜鉛表面に形成される薄い不
動態的皮膜を有するものでは、焼成時に不均一焼成とな
り、団魂状酸化亜鉛と金属亜鉛が共存するものとなる。
一方、上記の成長した酸化皮膜を有する亜鉛粉末では、
高温焼成が均一かつ完全に進行して、金属亜鉛は完全に
酸化されて、高率に酸化亜鉛ウィスカーに成長する。ま
た、高温焼成時、容器内部に設置した原料は容器内部で
反応が終結する。また、ここに生成するウィスカーは、
従来の酸化亜鉛ウィスカーにみられる単純な繊維状単結
晶体ではなく、核部から4軸に成長した針状結晶構造を
有するテトラポッド状構造を有する。As described above, an oxide film is formed on the surface of the zinc metal powder by applying mechanical pressure with a roller or the like in the presence of water as described above, but this film grows after being left in water later. . This was confirmed by the X-ray diffraction method. Further, the oxide film thus formed has a special effect. That is, in the case of a material having a thin passivation film that is usually formed on the surface of zinc in a dry atmosphere, it becomes non-uniformly fired at the time of firing, and zinc oxide and metallic zinc coexist.
On the other hand, in the zinc powder having the above grown oxide film,
The high temperature firing progresses uniformly and completely, the metallic zinc is completely oxidized, and the zinc oxide whiskers grow at a high rate. Further, during the high temperature firing, the reaction of the raw material placed inside the container is completed inside the container. Also, the whiskers generated here are
It is not a simple fibrous single crystal found in a conventional zinc oxide whisker, but has a tetrapod-like structure having a needle-like crystal structure grown from the nucleus in four axes.
この酸化亜鉛ウィスカーは、テトラポッド状構造が基本
形状であるが、3軸に成長した針状結晶構造を有するも
のが多い。これを二次加工、例えばボールミルで24時間
粉砕処理して結晶成長軸のつけ根部分より切断し、棒状
の針状酸化亜鉛とすることは勿論可能である。The zinc oxide whiskers have a tetrapod-like structure as a basic shape, but many of them have a triaxially grown needle-like crystal structure. It is, of course, possible to carry out secondary processing, for example, crushing with a ball mill for 24 hours and cutting from the root of the crystal growth axis to obtain rod-shaped acicular zinc oxide.
さて、この酸化亜鉛ウィスカーにガラスフリットを添加
し、このガラスフリットの融点以上の温度で焼成するこ
とにより過フィルターを得た。A glass frit was added to the zinc oxide whiskers and the mixture was baked at a temperature equal to or higher than the melting point of the glass frit to obtain an overfilter.
なお、酸化亜鉛ウィスカーの特性と量,ガラスフリット
の添加量と融点,焼成温度は以下の第1表の通りとし
た。The characteristics and amount of zinc oxide whiskers, the addition amount and melting point of glass frit, and the firing temperature were as shown in Table 1 below.
尚、実施例(1),(2),(3)共に成型時バインダ
ーとしてポリビニールアルコールを使用しプレス圧は20
0Kg/cm2とした。 In Examples (1), (2) and (3), polyvinyl alcohol was used as a binder at the time of molding and the pressing pressure was 20.
It was set to 0 kg / cm 2 .
以下の第2表は実施例(1),(2),(3)と従来例
(4),(5),(6)を一定条件で過実験を行い、
フィルター特性を検討した結果である。Table 2 below shows that Examples (1), (2) and (3) and Conventional Examples (4), (5) and (6) were subjected to over-experimentation under constant conditions.
This is the result of examining the filter characteristics.
(4),(5),(6)はそれぞれ紙,メンブランフ
ィルター,ニッケル焼結金属フィルターである。尚、フ
ィルター特性評価は純水に平均粒子径3μmのポリスチ
レンゲルを分散させて用いた。(4), (5) and (6) are a paper, a membrane filter and a nickel sintered metal filter, respectively. The filter characteristics were evaluated by using polystyrene gel having an average particle size of 3 μm dispersed in pure water.
以上の様に実施例は低圧下の透水性が大で、高圧下では
更に大きく変化して秀れたフィルター特性を示す。尚、
この時、この各フィルター共にポリスチレンゲルの拒絶
率は100%であった。 As described above, the examples have a large water permeability under low pressure, and further greatly change under high pressure, and show excellent filter characteristics. still,
At this time, the rejection rate of polystyrene gel was 100% in each of the filters.
発明の効果 以上のように本発明の過フィルターは高圧下でも極め
て安定で高透水性を示し過効率の著しい高いものであ
り、その産業性は大である。EFFECTS OF THE INVENTION As described above, the overfilter of the present invention is extremely stable even under high pressure, exhibits high water permeability, and has a significantly high overefficiency, and is highly industrial.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 朝倉 栄三 大阪府門真市大字門真1006番地 松下電器 産業株式会社内 (72)発明者 芳中 實 大阪府門真市大字門真1006番地 松下電器 産業株式会社内 (56)参考文献 特開 平1−215325(JP,A) ─────────────────────────────────────────────────── ─── Continuation of front page (72) Inventor Eizo Asakura 1006 Kadoma, Kadoma City, Osaka Prefecture Matsushita Electric Industrial Co., Ltd. (72) Minor Yoshinaka, 1006 Kadoma, Kadoma City, Osaka Matsushita Electric Industrial Co., Ltd. (56) References Japanese Patent Laid-Open No. 1-215325 (JP, A)
Claims (1)
鉛ウィスカーにガラスフリットを添加して焼成してなる
ことを特徴とする過フィルター。1. An overfilter which is obtained by adding glass frit to a zinc oxide whisker having a structure branched in two or more directions and firing the glass frit.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2310488A JPH07110326B2 (en) | 1988-02-02 | 1988-02-02 | ▲ Ro ▼ over filter |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2310488A JPH07110326B2 (en) | 1988-02-02 | 1988-02-02 | ▲ Ro ▼ over filter |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH01199618A JPH01199618A (en) | 1989-08-11 |
| JPH07110326B2 true JPH07110326B2 (en) | 1995-11-29 |
Family
ID=12101155
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2310488A Expired - Lifetime JPH07110326B2 (en) | 1988-02-02 | 1988-02-02 | ▲ Ro ▼ over filter |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH07110326B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4398142B2 (en) * | 2001-12-07 | 2010-01-13 | 日本碍子株式会社 | Porous ceramic body and method for producing glass used for the binder |
-
1988
- 1988-02-02 JP JP2310488A patent/JPH07110326B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH01199618A (en) | 1989-08-11 |
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