JPH04334552A - Composite photocatalytic material - Google Patents
Composite photocatalytic materialInfo
- Publication number
- JPH04334552A JPH04334552A JP3102496A JP10249691A JPH04334552A JP H04334552 A JPH04334552 A JP H04334552A JP 3102496 A JP3102496 A JP 3102496A JP 10249691 A JP10249691 A JP 10249691A JP H04334552 A JPH04334552 A JP H04334552A
- Authority
- JP
- Japan
- Prior art keywords
- light transmitting
- photocatalyst
- powder
- metal oxide
- oxide semiconductor
- 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.)
- Granted
Links
- 239000002131 composite material Substances 0.000 title claims abstract description 16
- 230000001699 photocatalysis Effects 0.000 title claims abstract description 13
- 239000000463 material Substances 0.000 title abstract description 9
- 239000011941 photocatalyst Substances 0.000 claims abstract description 23
- 229910044991 metal oxide Inorganic materials 0.000 claims abstract description 13
- 150000004706 metal oxides Chemical class 0.000 claims abstract description 13
- 239000000843 powder Substances 0.000 claims abstract description 13
- 239000004065 semiconductor Substances 0.000 claims abstract description 13
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 abstract description 22
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 17
- 239000010453 quartz Substances 0.000 abstract description 9
- 239000011347 resin Substances 0.000 abstract description 6
- 229920005989 resin Polymers 0.000 abstract description 6
- -1 perfluoroethylenepropylene Chemical group 0.000 abstract description 4
- 239000011521 glass Substances 0.000 abstract description 2
- 238000000151 deposition Methods 0.000 abstract 2
- GNTDGMZSJNCJKK-UHFFFAOYSA-N divanadium pentaoxide Chemical compound O=[V](=O)O[V](=O)=O GNTDGMZSJNCJKK-UHFFFAOYSA-N 0.000 abstract 2
- ZNOKGRXACCSDPY-UHFFFAOYSA-N tungsten(VI) oxide Inorganic materials O=[W](=O)=O ZNOKGRXACCSDPY-UHFFFAOYSA-N 0.000 abstract 1
- XLOMVQKBTHCTTD-UHFFFAOYSA-N zinc oxide Inorganic materials [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 abstract 1
- 238000006552 photochemical reaction Methods 0.000 description 5
- 229920000840 ethylene tetrafluoroethylene copolymer Polymers 0.000 description 3
- 229910010272 inorganic material Inorganic materials 0.000 description 3
- 239000011147 inorganic material Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 229910003074 TiCl4 Inorganic materials 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000003301 hydrolyzing effect Effects 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 2
- 229920001774 Perfluoroether Polymers 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000006722 reduction reaction Methods 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
- Surface Treatment Of Glass (AREA)
- Glass Compositions (AREA)
- Catalysts (AREA)
- Paints Or Removers (AREA)
- Treatment Of Water By Oxidation Or Reduction (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は光触媒複合材料に関し、
例えば脱硝装置、水処理装置、殺菌浄化装置などの光化
学反応系に適用される光触媒複合材料に関する。[Industrial Application Field] The present invention relates to a photocatalytic composite material.
For example, the present invention relates to photocatalytic composite materials that are applied to photochemical reaction systems such as denitrification equipment, water treatment equipment, and sterilization and purification equipment.
【0002】0002
【従来の技術】従来、金属酸化物半導体系光触媒として
はTiO2 ,V2 O5 ,ZnO,WO3 などが
知られているが、工業的には例えばTiO2 の場合、
光透過性多孔質石英板にTiCl4 を拡散吸着させ、
これを水蒸気で加水分解したのち、500〜700℃で
焼成し、TiO2 を担持して光透過性石英板として利
用されている。[Prior Art] Conventionally, TiO2, V2 O5, ZnO, WO3, etc. have been known as metal oxide semiconductor photocatalysts, but industrially, for example, in the case of TiO2,
TiCl4 is diffused and adsorbed onto a light-transmitting porous quartz plate.
After hydrolyzing this with steam, it is fired at 500 to 700°C to support TiO2 and is used as a light-transmitting quartz plate.
【0003】0003
【発明が解決しようとする課題】前記、従来の金属酸化
物半導体系光触媒を担持した光透過性石英板を工業的に
利用する場合には次の如き欠点がある。
(1)光化学反応効率を向上するためには前記石英板は
薄ければ薄い程よいことになるが、石英板は衝撃強度が
低く、僅かな衝撃によっても崩壊する。Problems to be Solved by the Invention When the above-mentioned conventional light-transmitting quartz plate supporting a metal oxide semiconductor photocatalyst is used industrially, there are the following drawbacks. (1) In order to improve the photochemical reaction efficiency, the thinner the quartz plate is, the better; however, the quartz plate has low impact strength and will collapse even with a slight impact.
【0004】(2)前記崩壊を防止するためには強度ア
ップのために、反応には利用されないにもかかわらず、
石英板を厚くするか、他の材料で周囲を補強する必要が
ある。(2) In order to prevent the collapse, in order to increase the strength, even though it is not used in the reaction,
It is necessary to make the quartz plate thicker or to reinforce the surrounding area with other materials.
【0005】(3)前記(1),(2)の如き欠点から
、工業的に重要となる大型の金属酸化物半導体系光触媒
を担持した光透過性石英板の製造が困難であり、大容量
の光化学反応プロセスへの適用は経済的にも問題がある
。(3) Due to the drawbacks mentioned in (1) and (2) above, it is difficult to manufacture a light-transmitting quartz plate supporting a large-sized metal oxide semiconductor photocatalyst, which is industrially important. The application of this to photochemical reaction processes is also economically problematic.
【0006】本発明は上記技術水準に鑑み、従来の光触
媒の有する不具合を解消した光触媒複合材料を提供しよ
うとするものである。[0006] In view of the above-mentioned state of the art, the present invention aims to provide a photocatalytic composite material that eliminates the problems of conventional photocatalysts.
【0007】[0007]
【課題を解決するための手段】本発明は金属酸化物半導
体系光触媒を担持した光透過性多孔質無機粉末を、光透
過性フッ素樹脂に熱溶着させてなることを特徴とする光
触媒複合材料である。本発明を更に具体的に述べると、
本発明は金属酸化物半導体系光触媒(TiO2 ,V2
O5 ,ZnO,WO3 など)を担持させた光透過
性多孔質無機材(石英,ガラスなど)を微細に粉砕する
か、もしくは予め微細に粉砕した前記光透過性多孔質無
機材に前記金属酸化物半導体系光触媒を担持させた粉末
を、光透過性フッ素樹脂〔パーフルオロエチレンプロピ
レン樹脂(FEP)、パーフルオロアルコキシ樹脂(P
FA)、エチレン−四フッ化エチレン樹脂(ETFE)
など〕のシート又は板の表面に加熱溶融させて付着させ
た光触媒複合材料である。[Means for Solving the Problems] The present invention is a photocatalytic composite material characterized by thermally welding a light-transmitting porous inorganic powder supporting a metal oxide semiconductor photocatalyst to a light-transmitting fluororesin. be. To describe the present invention more specifically,
The present invention uses metal oxide semiconductor photocatalysts (TiO2, V2
A light-transmissive porous inorganic material (quartz, glass, etc.) supporting O5, ZnO, WO3, etc.) is finely pulverized, or the metal oxide is applied to the light-transmissive porous inorganic material that has been finely ground in advance. The powder supporting the semiconductor photocatalyst is mixed with a light-transmitting fluororesin [perfluoroethylene propylene resin (FEP), perfluoroalkoxy resin (P
FA), ethylene-tetrafluoroethylene resin (ETFE)
It is a photocatalytic composite material that is heated and melted and attached to the surface of a sheet or plate.
【0008】[0008]
【作用】本発明は従来の光触媒の欠点を解消するため、
金属酸化物半導体系光触媒を担持した光透過性多孔質無
機材には光触媒としての機能のみをもたせ、強度が要求
される補強材に衝撃強度の強い光透過性フッ素樹脂を利
用したものである。[Operation] In order to eliminate the drawbacks of conventional photocatalysts, the present invention
The light-transparent porous inorganic material supporting the metal oxide semiconductor photocatalyst has only the function of a photocatalyst, and a light-transparent fluororesin with high impact strength is used as a reinforcing material that requires strength.
【0009】本発明は金属酸化物半導体系光触媒を担持
させた光透過性多孔質無機粉末を用いるため、従来の板
材に担持させたものに比べて、光化学反応に有効な活性
点を多く利用できる利点を有し、かつ紫外線の透過率の
高いフッ素樹脂フィルム又はシートを用いているため、
光エネルギーの減衰も少なく、エネルギー効率も高い。[0009] Since the present invention uses a light-transmissive porous inorganic powder supporting a metal oxide semiconductor photocatalyst, more active sites effective for photochemical reactions can be utilized than in the case of a conventional plate material supporting the photocatalyst. Because it uses a fluororesin film or sheet that has the advantages and high transmittance of ultraviolet rays,
It also has low attenuation of light energy and high energy efficiency.
【0010】0010
【実施例】以下、本発明の実施例を図1及び図2によっ
て説明する。図1は金属酸化物半導体系光触媒として平
均粒径10μmのTiO2 系光触媒を担持した多孔質
石英ガラス粉末1を100μmのフッ素樹脂フィルム2
に熱融着させた本発明の一実施態様を示す断面図である
。
図2は100μmのフッ素樹脂フィルム2の両面に平均
粒径10μmのTiO2 光触媒を担持した多孔質石英
ガラス粉末1を熱融着した断面図である。Embodiments Hereinafter, embodiments of the present invention will be explained with reference to FIGS. 1 and 2. Figure 1 shows a porous quartz glass powder 1 supporting a TiO2 photocatalyst with an average particle size of 10 μm as a metal oxide semiconductor photocatalyst, and a 100 μm fluororesin film 2.
FIG. 2 is a cross-sectional view showing an embodiment of the present invention heat-sealed to. FIG. 2 is a cross-sectional view of a 100 μm fluororesin film 2 and a porous quartz glass powder 1 carrying a TiO2 photocatalyst with an average particle size of 10 μm, which is thermally fused on both sides.
【0011】図1,図2に示す本発明の光触媒複合材料
のTiO2 系光触媒を担持した多孔質石英ガラス粉末
1は多孔質石英ガラス板材にTiCl4 を吸着させて
から、180℃で加水分解後、600℃で焼成し、これ
を10μmまで粉砕したものを用いた。The porous quartz glass powder 1 supporting the TiO2-based photocatalyst of the photocatalytic composite material of the present invention shown in FIGS. 1 and 2 is prepared by adsorbing TiCl4 onto a porous quartz glass plate, and then hydrolyzing it at 180°C. The material was fired at 600°C and ground to 10 μm.
【0012】上記方法で作成した粉末1を350〜40
0℃に加熱し、融点よりも50〜100℃低い温度に加
熱した100μmのFEPフィルム,PFAフィルム,
ETFEフィルムに散布したのち、ロールで圧縮し、T
iO2 を担持した多孔質石英ガラス粉末1をフッ素樹
脂フィルム2の表面に熱融着させて、TiO2 光触媒
を熱融着させたフッ素樹脂複合材料を作成した。[0012] Powder 1 prepared by the above method was 350 to 40
100μm FEP film, PFA film heated to 0℃ and heated to a temperature 50 to 100℃ lower than the melting point,
After spraying on ETFE film, it is compressed with a roll and T
Porous quartz glass powder 1 supporting iO2 was thermally fused to the surface of a fluororesin film 2, thereby creating a fluororesin composite material to which a TiO2 photocatalyst was thermally fused.
【0013】前記方法で作成したTiO2 光触媒を熱
融着させたフッ素樹脂複合材料の長さ280mm×幅3
0mmのシートを低圧Hgランプを設置した光化学反応
容器(長さ280mm×幅30mm×高さ20mm)に
セットし、20℃でHeにNO 470ppmを混合
したガスを100ml/min の速度で流通し、NO
の還元反応を行った。その結果は100μmのTiO2
光触媒を担持した多孔質石英ガラス板で行った試験に
おける反応率、エネルギー効率とほぼ同等であった。[0013] The fluororesin composite material prepared by the above method and heat-sealed with TiO2 photocatalyst has a length of 280 mm and a width of 3
A 0 mm sheet was set in a photochemical reaction vessel (length 280 mm x width 30 mm x height 20 mm) equipped with a low-pressure Hg lamp, and a gas containing 470 ppm of He and NO mixed at 20 °C was passed through at a rate of 100 ml/min. NO
A reduction reaction was performed. The result is 100μm TiO2
The reaction rate and energy efficiency were almost the same as in a test conducted using a porous quartz glass plate supporting a photocatalyst.
【0014】[0014]
【発明の効果】本発明は柔軟性があって衝撃力にも強い
光透過性フッ素樹脂を基材に用いており、従来の石英ガ
ラス板のように崩壊しがたく、連続した大型の複合材料
も安価に製造できる。更に反応器の形状によっては任意
の形状に変えることができるなど、工業的価値は大きい
。[Effect of the invention] The present invention uses a light-transmitting fluororesin that is flexible and strong against impact as a base material, and is a continuous large composite material that does not easily collapse like conventional quartz glass plates. can also be manufactured cheaply. Furthermore, depending on the shape of the reactor, it can be changed to any shape, which has great industrial value.
【図1】本発明の光触媒複合材料の一実施例の断面図。FIG. 1 is a sectional view of an example of the photocatalytic composite material of the present invention.
【図2】本発明の光触媒複合材料の他の実施例の断面図
。FIG. 2 is a sectional view of another example of the photocatalytic composite material of the present invention.
Claims (1)
光透過性多孔質無機粉末を、光透過性フッ素樹脂に熱溶
着させてなることを特徴とする光触媒複合材料。1. A photocatalytic composite material comprising a light-transparent porous inorganic powder supporting a metal oxide semiconductor photocatalyst and heat-welded to a light-transparent fluororesin.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3102496A JP2971169B2 (en) | 1991-05-08 | 1991-05-08 | Photocatalytic composite material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3102496A JP2971169B2 (en) | 1991-05-08 | 1991-05-08 | Photocatalytic composite material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH04334552A true JPH04334552A (en) | 1992-11-20 |
| JP2971169B2 JP2971169B2 (en) | 1999-11-02 |
Family
ID=14329026
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3102496A Expired - Fee Related JP2971169B2 (en) | 1991-05-08 | 1991-05-08 | Photocatalytic composite material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2971169B2 (en) |
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0760132A (en) * | 1993-08-24 | 1995-03-07 | Matsushita Seiko Co Ltd | Photocatalyst and method for carrying the same |
| JPH07148434A (en) * | 1993-07-12 | 1995-06-13 | Ishihara Sangyo Kaisha Ltd | Photocatalyst and water cleaning method using the same |
| US5547823A (en) * | 1993-06-28 | 1996-08-20 | Ishihara Sangyo Kaisha, Ltd. | Photocatalyst composite and process for producing the same |
| JPH08243402A (en) * | 1995-03-08 | 1996-09-24 | Nippon Insulation Kk | Photocatalst material and its manufacture |
| US5616532A (en) * | 1990-12-14 | 1997-04-01 | E. Heller & Company | Photocatalyst-binder compositions |
| JPH09173783A (en) * | 1995-10-27 | 1997-07-08 | Matsushita Electric Ind Co Ltd | Flat glass, resin plate, manufacturing method thereof and pollutant removal method |
| JPH09313887A (en) * | 1996-05-28 | 1997-12-09 | Agency Of Ind Science & Technol | Photocatalyst sheet |
| US5849200A (en) * | 1993-10-26 | 1998-12-15 | E. Heller & Company | Photocatalyst-binder compositions |
| JP2000197824A (en) * | 1999-01-08 | 2000-07-18 | Kawasaki Steel Corp | Air purification material |
| US6107241A (en) * | 1996-03-29 | 2000-08-22 | Tao Inc. | Photocatalytic body and method for making same |
| CN102964066A (en) * | 2011-11-17 | 2013-03-13 | 天津法莫西医药科技有限公司 | Template-free method for preparation of zinc oxide nano-arrays growing on hollow glass bead surfaces |
-
1991
- 1991-05-08 JP JP3102496A patent/JP2971169B2/en not_active Expired - Fee Related
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5616532A (en) * | 1990-12-14 | 1997-04-01 | E. Heller & Company | Photocatalyst-binder compositions |
| US6277346B1 (en) | 1993-06-28 | 2001-08-21 | Ishihara Sangyo Kaisha, Ltd. | Photocatalyst composite and process for producing the same |
| US6498000B2 (en) | 1993-06-28 | 2002-12-24 | Ishihara Sangyo Kaisha, Ltd. | Photocatalyst composite and process for producing the same |
| US5547823A (en) * | 1993-06-28 | 1996-08-20 | Ishihara Sangyo Kaisha, Ltd. | Photocatalyst composite and process for producing the same |
| JPH07148434A (en) * | 1993-07-12 | 1995-06-13 | Ishihara Sangyo Kaisha Ltd | Photocatalyst and water cleaning method using the same |
| JPH0760132A (en) * | 1993-08-24 | 1995-03-07 | Matsushita Seiko Co Ltd | Photocatalyst and method for carrying the same |
| US6093676A (en) * | 1993-10-26 | 2000-07-25 | E. Heller & Company | Photocatalyst-binder compositions |
| US5854169A (en) * | 1993-10-26 | 1998-12-29 | E. Heller & Company | Photocatalyst-binder compositions |
| US5849200A (en) * | 1993-10-26 | 1998-12-15 | E. Heller & Company | Photocatalyst-binder compositions |
| JPH08243402A (en) * | 1995-03-08 | 1996-09-24 | Nippon Insulation Kk | Photocatalst material and its manufacture |
| JPH09173783A (en) * | 1995-10-27 | 1997-07-08 | Matsushita Electric Ind Co Ltd | Flat glass, resin plate, manufacturing method thereof and pollutant removal method |
| US6107241A (en) * | 1996-03-29 | 2000-08-22 | Tao Inc. | Photocatalytic body and method for making same |
| US6429169B1 (en) | 1996-03-29 | 2002-08-06 | Saga-Ken | Photocatalytic body and method for making same |
| JPH09313887A (en) * | 1996-05-28 | 1997-12-09 | Agency Of Ind Science & Technol | Photocatalyst sheet |
| JP2000197824A (en) * | 1999-01-08 | 2000-07-18 | Kawasaki Steel Corp | Air purification material |
| CN102964066A (en) * | 2011-11-17 | 2013-03-13 | 天津法莫西医药科技有限公司 | Template-free method for preparation of zinc oxide nano-arrays growing on hollow glass bead surfaces |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2971169B2 (en) | 1999-11-02 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 19990803 |
|
| LAPS | Cancellation because of no payment of annual fees |