JPH10137329A - Air purifying film and its manufacture - Google Patents

Air purifying film and its manufacture

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Publication number
JPH10137329A
JPH10137329A JP8304274A JP30427496A JPH10137329A JP H10137329 A JPH10137329 A JP H10137329A JP 8304274 A JP8304274 A JP 8304274A JP 30427496 A JP30427496 A JP 30427496A JP H10137329 A JPH10137329 A JP H10137329A
Authority
JP
Japan
Prior art keywords
film
adsorbent
photocatalyst
performance
air purification
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
Application number
JP8304274A
Other languages
Japanese (ja)
Inventor
Kazuo Nishikawa
和男 西川
Yasuaki Sakane
安昭 坂根
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sharp Corp
Original Assignee
Sharp Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Sharp Corp filed Critical Sharp Corp
Priority to JP8304274A priority Critical patent/JPH10137329A/en
Publication of JPH10137329A publication Critical patent/JPH10137329A/en
Pending legal-status Critical Current

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  • Disinfection, Sterilisation Or Deodorisation Of Air (AREA)

Abstract

PROBLEM TO BE SOLVED: To improve the decomposing activity of an odor component adsorbed to a coating film surface and suppress the desorption of aldehyde having low adsorptive performance by providing a lower film containing an adsorbent, or an optical catalyst and the adsorbent, and an upper film covering the lower film and containing the optical catalyst in a quantity larger to the adsorbent than the lower film. SOLUTION: An air purifying film is formed of a bed film 2 formed on the surface of a base 1, and an overcoat film 3 formed on the surface thereof. Each of the films 3, 2 contains an adsorbent 4, an optical catalyst 5 and a binder 6, and the optical catalyst 5 of the overcoat film 3 is contained in a quantity larger than the optical catalyst 5 of the bed film 2. Thus, the decomposing performance by the optical catalyst 5 in the overcoat film 3 surface and the critical surface between the film 3 and the bed film 2 is enhanced to raise the decomposing performance of the adsorbed component and the regenerating performance of the adsorbent 4, so that the adsorptive performance can be kept for a long time. Since the odor component adsorbed by the bed film 2 is necessarily passed through the overcoat film 3 even if desorpted from the adsorbent 4, the odor can be efficiently decomposed by ultraviolet rays.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、空気中に含まれる
臭気を浄化する膜に関し、特に臭気成分として、NOx
及び有機化合物等を含む空気を浄化するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a membrane for purifying odors contained in air, and more particularly, to a membrane containing NOx as an odor component.
And air containing organic compounds and the like.

【0002】[0002]

【従来の技術】従来の光触媒を用いた脱臭装置として
は、特開平5―293165号公報に開示されるよう
に、活性炭と光触媒とを複合化したものが提案されてお
り、これを図12に示す。
2. Description of the Related Art As a conventional deodorizing apparatus using a photocatalyst, a composite of activated carbon and a photocatalyst has been proposed as disclosed in JP-A-5-293165, which is shown in FIG. Show.

【0003】図12において、光源からの光を遮光する
フィルタ102と、光触媒を励起させる紫外線ランプ1
03と、光触媒付吸着活性炭104と、送風手段105
とがこの順に直列に配設される。送風機105を所定時
間稼働させた後、送風機105を止め、光源を所定時間
点灯させて、光触媒付吸着活性炭104の再活性化を行
い、その後自動的に電源の供給を遮断する。
In FIG. 12, a filter 102 for blocking light from a light source and an ultraviolet lamp 1 for exciting a photocatalyst are shown.
03, adsorption activated carbon 104 with photocatalyst, and blowing means 105
Are arranged in series in this order. After operating the blower 105 for a predetermined time, the blower 105 is stopped, the light source is turned on for a predetermined time, the activated activated carbon 104 with photocatalyst is reactivated, and then the power supply is automatically cut off.

【0004】上記構成により、紫外線ランプ103を用
いて光触媒付吸着活性炭104の表面の光触媒を励起さ
せ、光触媒により光触媒付吸着活性炭104が吸着した
臭いの成分を分解させるものである。
With the above structure, the ultraviolet light lamp 103 is used to excite the photocatalyst on the surface of the activated carbon with photocatalyst 104, and the photocatalyst decomposes the odor component adsorbed by the activated carbon with photocatalyst 104.

【0005】[0005]

【発明が解決しようとする課題】しかしながら、上記し
た従来の空気浄化塗膜では、光触媒付吸着活性炭104
等の吸着剤の表面に光触媒のみの膜が形成されている
と、光触媒の臭い成分に対する吸着性能は、光触媒の種
類により異なり、特に酸化チタンでは臭い成分を分解す
る際に中間生成物としてアルデヒド類が生成されると、
アルデヒド類が酸化チタンの表面から脱離を起こし空気
中に放出される問題があった。
However, in the above-mentioned conventional air purification coating film, the adsorption activated carbon 104 with a photocatalyst is used.
If a film consisting only of a photocatalyst is formed on the surface of an adsorbent such as, the adsorption performance of the photocatalyst for odor components differs depending on the type of photocatalyst. Particularly, titanium dioxide decomposes aldehydes as intermediate products when decomposing odor components. Is generated,
There has been a problem that aldehydes desorb from the surface of titanium oxide and are released into the air.

【0006】本発明は、上記課題を解決するものであ
り、光触媒による塗膜表面に吸着された臭い成分の分解
活性を向上させ、同時に、光触媒では吸着性能の低いア
ルデヒド類の脱離を抑える空気浄化膜を提供することを
目的とする。
SUMMARY OF THE INVENTION The present invention has been made to solve the above-mentioned problems, and it is an object of the present invention to improve the activity of decomposing odor components adsorbed on the surface of a coating film by a photocatalyst, and at the same time, to suppress the desorption of aldehydes having a low adsorption performance with a photocatalyst. It is intended to provide a purification membrane.

【0007】[0007]

【課題を解決するための手段】上記課題を解決するため
に本発明は、吸着剤、もしくは、光触媒と吸着剤を複合
した下地膜(下膜)の表面に、下膜より光触媒の配合比
が大きいオーバーコート膜(上膜)を形成した多膜の空
気浄化膜である。まず、下地膜の塗液を、基材となる各
種材料のシートまたはハニカム等の通気性担体に塗布
し、乾燥・焼付けを行い下地膜を作成する。さらに、下
地膜上に吸着剤として銅イオン交換処理をしたハイシリ
カ合成ゼオライトH型ZSM5を用いたオーバーコート
膜の塗液を塗布、乾燥、焼付けの処理を行い、多層の空
気浄化塗膜を形成させる。この膜に接触する空気の汚れ
成分は吸着され、膜に紫外線を照射することにより光触
媒を励起させ、吸着された成分を分解する。
SUMMARY OF THE INVENTION In order to solve the above-mentioned problems, the present invention provides an adsorbent or a base film (lower film) in which a photocatalyst and an adsorbent are combined to form a photocatalyst at a lower mixing ratio than the lower film. This is a multi-layer air purification film on which a large overcoat film (upper film) is formed. First, the coating liquid for the base film is applied to a sheet of various materials serving as a base material or a gas-permeable carrier such as a honeycomb, and dried and baked to form a base film. Further, a coating solution for an overcoat film using high silica synthetic zeolite H-type ZSM5, which has been subjected to a copper ion exchange treatment as an adsorbent, is applied to the base film, dried and baked to form a multilayer air purification coating film. . The dirt component of the air that comes into contact with this film is adsorbed, and the film is irradiated with ultraviolet light to excite the photocatalyst and decompose the adsorbed component.

【0008】[0008]

【発明の実施の形態】以下、本発明の空気浄化膜に係る
実施の形態について、図面を参照しながら説明する。本
発明の空気浄化膜の実施の形態は、下地膜(下膜)の表
面にオーバーコート膜(上膜)を形成したものである。
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS Hereinafter, embodiments of the air purification membrane of the present invention will be described with reference to the drawings. In the embodiment of the air purification film of the present invention, an overcoat film (upper film) is formed on the surface of a base film (lower film).

【0009】本発明の空気浄化膜のオーバーコート膜に
おける適切な光触媒と吸着剤との配合比を求めるべく、
光触媒と吸着剤との配合比を種々変更して一層の膜を形
成した。光触媒としては、石原産業株式会社製の酸化チ
タンST―01を用い、吸着剤としては、銅イオン交換
処理を施したハイシリカ合成ゼオライトH型ZSM5を
用い、バインダーとしてテルニック工業株式会社製のコ
ロイダルシリカ系バインダー、ベタックNo970GD
改(商品名)を用いた。
In order to determine an appropriate mixing ratio of the photocatalyst and the adsorbent in the overcoat film of the air purification film of the present invention,
Various layers were formed by changing the mixing ratio of the photocatalyst and the adsorbent. As a photocatalyst, titanium oxide ST-01 manufactured by Ishihara Sangyo Co., Ltd. is used. As an adsorbent, high silica synthetic zeolite H type ZSM5 subjected to a copper ion exchange treatment is used. Binder, Bettac No 970GD
Kai (product name) was used.

【0010】また、バインダーの固形分比(重量比)を
50%とし、光触媒と吸着剤との和の固形分比を50%
とし、光触媒と吸着剤との比を50%の範囲内で、表1
に示すように種々変更して、200×90×t20(m
m)のアルミコルゲートハニカム(200セル/inc
2 )の表面に、200(g/l)になるように塗布
し、380℃で1時間焼付けを行ってサンプルA〜Dを
作成した。
The solid content ratio (weight ratio) of the binder is set to 50%, and the solid content ratio of the sum of the photocatalyst and the adsorbent is set to 50%.
And the ratio between the photocatalyst and the adsorbent was within a range of 50%.
Are variously changed as shown in FIG.
m) aluminum corrugated honeycomb (200 cells / inc)
Samples A to D were prepared by applying 200 (g / l) to the surface of h 2 ) and baking at 380 ° C. for 1 hour.

【0011】[0011]

【表1】 [Table 1]

【0012】これらのサンプルを1(m3 )のボックス
内に設置し、乾燥した清浄空気をパージして臭気等を除
いた後、ボックス内でマイルドセブン5本を同時に燃焼
させ、風量0.94(m3 /min)をとして、空気浄
化を行いながらサンプルに紫外線3.4(mW/cm
2 )を照射し、ガス検知管によリアセトアルデヒド(図
1に示す)およびNOx(図2に示す)の脱臭性能を測
定した。
After placing these samples in a 1 (m 3 ) box and purging dry clean air to remove odors and the like, five mild sevens were simultaneously burned in the box, and the air flow was 0.94 (m 3 ). m 3 / min), the sample was irradiated with ultraviolet light 3.4 (mW / cm) while performing air purification.
2 ), and the deodorizing performance of liacetaldehyde (shown in FIG. 1) and NOx (shown in FIG. 2) was measured by a gas detector tube.

【0013】図1に示すように、アセトアルデヒドの残
存率は、サンプルBがもっとも早く低下し、次にサンプ
ルA,サンプルCがアセトアルデヒドの残存率を低く保
てたが、サンプルDは、吸着剤を含まないため、臭気の
分解により光触媒から発生したアセトアルデヒドが、触
媒膜から離脱した。これによって吸着剤含まないサンプ
ルDは不適切であることがわかった。また、図2に示す
ように、吸着剤に対する光触媒の比が大きいほど、一酸
化窒素の残存率は早く低下した。しかし、サンプルA
は、100分経過した時点でも、10%程度の一酸化窒
素が残存するため、サンプルAは不適切であることがわ
かった。図1及び図2に示す結果より、オーバーコート
膜に適切な光触媒と吸着剤との比は、1:9〜1:49
であることがわかった。
As shown in FIG. 1, the residual ratio of acetaldehyde was reduced most rapidly in sample B, and then the residual ratio of acetaldehyde was kept low in samples A and C, but in sample D, the adsorbent was not used. Since it did not contain, acetaldehyde generated from the photocatalyst by decomposition of the odor was separated from the catalyst film. This indicated that Sample D without adsorbent was unsuitable. In addition, as shown in FIG. 2, the larger the ratio of the photocatalyst to the adsorbent, the faster the residual rate of nitric oxide decreased. However, sample A
The sample A was found to be unsuitable because about 10% of nitric oxide remained even after 100 minutes. From the results shown in FIGS. 1 and 2, the ratio of the photocatalyst to the adsorbent suitable for the overcoat film is 1: 9 to 1:49.
It turned out to be.

【0014】以上の結果をまとめると、光触媒のみで
は、アセトアルデヒドの脱臭性能が低いため、臭気成分
の分解時に中間生成物としてアセトアルデヒドが生成す
ると、光触媒からのアセトアルデヒドの離脱が起こる。
しかし、図1に示すように、光触媒に吸着剤を加えるこ
と(サンプルA〜C)により、アセトアルデヒドの空気
中への離脱を抑えることができ、また、吸着剤と光触媒
との比が1:1(サンプルA)では一酸化窒素(NO
x)の脱臭性能が低いため、光触媒と吸着剤の配合比を
1:9〜1:49に調整することにより、NOxの脱臭
性能をあげかつ、アセトアルデヒドの残存率を低下させ
ることができた。
Summarizing the above results, the deodorizing performance of acetaldehyde is low with the photocatalyst alone, and if acetaldehyde is generated as an intermediate during decomposition of the odor component, the acetaldehyde is released from the photocatalyst.
However, as shown in FIG. 1, by adding an adsorbent to the photocatalyst (samples A to C), the release of acetaldehyde into the air can be suppressed, and the ratio of the adsorbent to the photocatalyst is 1: 1. (Sample A) contains nitric oxide (NO
Since the deodorizing performance of x) is low, the deodorizing performance of NOx can be improved and the residual ratio of acetaldehyde can be reduced by adjusting the mixing ratio of the photocatalyst and the adsorbent to 1: 9 to 1:49.

【0015】以下、上記した光触媒と吸着剤との比のデ
ータに基いて、下地膜(下膜)の表面にオーバーコート
膜(上膜)を形成した本発明の空気浄化膜の実施の形態
を説明する。
Hereinafter, an embodiment of the air purification film of the present invention in which an overcoat film (upper film) is formed on the surface of a base film (lower film) based on the data of the ratio between the photocatalyst and the adsorbent will be described. explain.

【0016】光触媒、吸着剤、バインダーは、上記した
ものと同一のものを用いる。先ず、光触媒の固形分比
(重量比)を25%、吸着剤の固形分比を25%、バイ
ンダーの固形分比を50%とした下地膜用塗液を作成
し、この塗液を基材となるアルミコルゲートハニカムの
表面に、200(g/l)になるように塗布し、380
℃で1時間焼付けを行って下地膜を形成した。
The same photocatalyst, adsorbent and binder are used as described above. First, a coating solution for a base film was prepared in which the solid content ratio (weight ratio) of the photocatalyst was 25%, the solid content ratio of the adsorbent was 25%, and the solid content ratio of the binder was 50%. Is applied to the surface of the aluminum corrugated honeycomb to be 200 (g / l) to be 380
The substrate was baked at 1 ° C. for 1 hour to form a base film.

【0017】さらに、光触媒の固形分比49%、吸着剤
の固形分比1%、バインダーの固形分比50%(即ち、
サンプルC)のオーバーコート膜用塗液を作成して、こ
の塗液を下地膜表面にオーバーコートして、380℃で
1時間焼付けを行って、オーバーコート膜と下地膜とか
ら構成される空気浄化膜のサンプルE〜Gを作成した。
なお、サンプルE〜Gは下地膜に対するオーバーコート
膜の重量比を、表2に示すように種々変更したものであ
る。
Furthermore, the solid content ratio of the photocatalyst is 49%, the solid content ratio of the adsorbent is 1%, and the solid content ratio of the binder is 50% (that is, the solid content ratio is 50%).
A coating solution for the overcoat film of sample C) is prepared, and the coating solution is overcoated on the surface of the undercoat film and baked at 380 ° C. for 1 hour to form an air composed of the overcoat film and the undercoat film. Purification membrane samples EG were prepared.
Samples E to G were obtained by changing the weight ratio of the overcoat film to the base film as shown in Table 2.

【0018】[0018]

【表2】 [Table 2]

【0019】下地膜の表面にオーバーコート膜を形成し
た空気浄化膜の膜構造を、図3に示す。図3において、
空気浄化膜の構造は、基材1の表面に下地膜2を形成
し、さらに該下地膜2の表面にオーバーコート膜3を形
成する。また、オーバーコート膜3,下地膜2には、そ
れぞれ吸着剤4,光触媒5,バインダー6が含まれてお
り、オーバーコート膜3に含まれる光触媒5は、下地膜
2に含まれる光触媒5よりも多く含まれている。
FIG. 3 shows a film structure of an air purification film in which an overcoat film is formed on the surface of a base film. In FIG.
The structure of the air purification film is such that a base film 2 is formed on the surface of a base material 1 and an overcoat film 3 is formed on the surface of the base film 2. The overcoat film 3 and the base film 2 include the adsorbent 4, the photocatalyst 5, and the binder 6, respectively. The photocatalyst 5 included in the overcoat film 3 is more than the photocatalyst 5 included in the base film 2. Many are included.

【0020】上記したサンプルE〜Gを1(m3 )のボ
ックス内に設置し、乾燥した清浄空気をパージした後、
マイルドセブン5本を同時に燃焼させ、風量0.94
(m3/min)で空気浄化を行いながら各サンプルに
紫外線3.4(mW/cm2 )を照射し、ガス検知管に
より、アセトアルデヒド(図4)、NOx(図5)、一
酸化炭素(図6)、スチレン(図7)、酢酸(図8)、
アンモニア(図9)及びピリジン(図10)の脱臭性能
(分解性能)を測定した。
The above-mentioned samples EG were placed in a box of 1 (m 3 ), and after purging dry clean air,
Simultaneously burn five mild sevens, air volume 0.94
Each sample was irradiated with ultraviolet light 3.4 (mW / cm 2 ) while purifying air at (m 3 / min), and acetaldehyde (FIG. 4), NOx (FIG. 5), carbon monoxide ( FIG. 6), styrene (FIG. 7), acetic acid (FIG. 8),
The deodorizing performance (decomposition performance) of ammonia (FIG. 9) and pyridine (FIG. 10) was measured.

【0021】図4に示すように、アセトアルデヒドの残
存率は、サンプルE,Fが時間とともに低下したが、サ
ンプルGは、アセトアルデヒドの残存率が時間の経過に
より一定の値になってしまった。図5に示すように、N
Oxとして代表的な一酸化窒素の残存率は、サンプル
E,Fがよい値を示したが、サンプルGでは100分の
時点でも一酸化窒素が30%以上残っていた。
As shown in FIG. 4, the residual ratio of acetaldehyde in Samples E and F decreased with time, but in Sample G, the residual ratio of acetaldehyde became constant over time. As shown in FIG.
Samples E and F showed good values of the residual ratio of nitric oxide representative of Ox, but in Sample G, 30% or more of nitric oxide remained even at 100 minutes.

【0022】図6に示すように、一酸化炭素の残存率
は、サンプルE,F,Gの何れも大差がなかった。図7
に示すように、スチレンの残存率は、サンプルE,Fは
時間とともに低下したが、サンプルGは、スチレンの残
存率が時間の経過により一定の値になってしまった。図
8、図9、図10に示すように、酢酸、アンモニア、ピ
リジンの残存率は、それぞれサンプルE,F,Gの何れ
も大差がなかった。
As shown in FIG. 6, the residual ratio of carbon monoxide was not significantly different in any of Samples E, F and G. FIG.
As shown in Table 2, the residual ratio of styrene decreased with time in Samples E and F, but in Sample G, the residual ratio of styrene became constant over time. As shown in FIGS. 8, 9, and 10, the residual ratios of acetic acid, ammonia, and pyridine did not differ significantly among samples E, F, and G, respectively.

【0023】上記の結果により、サンプルE,F、即
ち、オーバーコート膜と下地膜との担持量比(重量比)
を、1:2〜1:4とした場合に、種々臭気を吸着分解
可能となった。
From the above results, the carrying ratio (weight ratio) of Samples E and F, that is, the overcoat film and the base film.
When the ratio was 1: 2 to 1: 4, various odors could be adsorbed and decomposed.

【0024】なお、図11に示すように、吸着剤の選択
は光触媒による分解効率の低いアセトアルデヒドに対し
て吸着性能の高いものとして、ハイシリカ合成ゼオライ
トH型ZSM5を銅イオン交換処理を施したCu−ZS
M5を用いた。
As shown in FIG. 11, the selection of the adsorbent was made on the assumption that the adsorbent had a high adsorption performance for acetaldehyde having a low decomposition efficiency by the photocatalyst, and the high silica synthetic zeolite H-type ZSM5 was subjected to a copper ion exchange treatment. ZS
M5 was used.

【0025】[0025]

【発明の効果】本発明の空気浄化膜は上記のような構成
であるため、請求項1によれば、上膜表面及び上膜と下
膜との界面での光触媒による分解性能を高め、吸着した
成分の分解及び吸着剤の再生能力が上がり、吸着性能を
長時間維持できる。また、下膜に吸着された臭気成分
は、吸着剤から脱離しても必ず上膜を通過するため、紫
外線により効率良く臭気を分解できる。
According to the first aspect of the present invention, the air purifying film of the present invention has the above-mentioned structure, so that the photocatalytic decomposition performance at the surface of the upper film and at the interface between the upper film and the lower film is enhanced, and the adsorption is improved. The ability to decompose the components and regenerate the adsorbent is increased, and the adsorption performance can be maintained for a long time. Further, the odor component adsorbed on the lower film always passes through the upper film even if it is desorbed from the adsorbent, so that the odor can be efficiently decomposed by ultraviolet rays.

【0026】請求項2によれば、上膜の光触媒と吸着剤
との比を操作することにより、光触媒単独では吸着性能
が低いアルデヒド類の成分の吸着性能を下膜で高めるこ
とができ、アルデヒド類の空気浄化膜からの脱離を抑え
る。また、上膜に含まれる光触媒により吸着剤単独では
脱臭が困難であったNOxの脱臭が可能となる。
According to the second aspect, by controlling the ratio of the photocatalyst to the adsorbent in the upper film, the adsorption performance of the aldehyde components having low adsorption performance by the photocatalyst alone can be enhanced in the lower film. To prevent desorption from the air purification membrane. In addition, the photocatalyst contained in the upper film makes it possible to deodorize NOx, which was difficult to deodorize with the adsorbent alone.

【0027】請求項3によれば、上膜と下膜との重量比
を操作することにより、下膜における吸着量が増加す
る。
According to the third aspect, by controlling the weight ratio between the upper film and the lower film, the amount of adsorption on the lower film is increased.

【0028】請求項4によれば、光触媒のみでは吸着性
能が低いアルデヒド類に対する吸着性能が向上するた
め、吸着剤に対する光触媒の配合比を大きくすることが
でき、分解効率を向上することができる。
According to the fourth aspect, since the adsorption performance of aldehydes having low adsorption performance with the photocatalyst alone is improved, the mixing ratio of the photocatalyst to the adsorbent can be increased, and the decomposition efficiency can be improved.

【0029】請求項5によれば、種々の臭気を吸着分解
できる空気浄化膜を製造できる。
According to the fifth aspect, an air purification membrane capable of adsorbing and decomposing various odors can be manufactured.

【図面の簡単な説明】[Brief description of the drawings]

【図1】本発明のために光触媒と吸着剤との比を変更し
た一層の膜によるアセトアルデヒド浄化性能を示す説明
図である。
FIG. 1 is an explanatory diagram showing acetaldehyde purification performance by a single layer film in which the ratio between a photocatalyst and an adsorbent is changed for the present invention.

【図2】図1の一層の膜による―酸化窒素浄化性能を示
す説明図である。
FIG. 2 is an explanatory view showing a nitrogen oxide purification performance by a single layer of FIG. 1;

【図3】本発明の空気浄化膜の実施形態の膜構造を示す
断面図である。
FIG. 3 is a sectional view showing a film structure of an embodiment of the air purification film of the present invention.

【図4】本発明の空気浄化膜の実施形態によるアセトア
ルデヒド浄化性能を示す説明図である。
FIG. 4 is an explanatory view showing acetaldehyde purification performance according to an embodiment of the air purification membrane of the present invention.

【図5】本発明の空気浄化膜の実施形態による一酸化窒
素浄化性能を示す説明図である。
FIG. 5 is an explanatory diagram showing nitric oxide purification performance according to an embodiment of the air purification membrane of the present invention.

【図6】本発明の空気浄化膜の実施形態による一酸化炭
素浄化性能を示す説明図である。
FIG. 6 is an explanatory diagram showing carbon monoxide purification performance according to an embodiment of the air purification membrane of the present invention.

【図7】本発明の空気浄化膜の実施形態によるスチレン
浄化性能を示す説明図である。
FIG. 7 is an explanatory diagram showing styrene purification performance according to an embodiment of the air purification membrane of the present invention.

【図8】本発明の空気浄化膜の実施形態による酢酸浄化
性能を示す説明図である。
FIG. 8 is an explanatory diagram showing acetic acid purification performance according to an embodiment of the air purification membrane of the present invention.

【図9】本発明の空気浄化膜の実施形態によるアンモニ
ア浄化性能を示す説明図である。
FIG. 9 is an explanatory diagram showing ammonia purification performance according to an embodiment of the air purification film of the present invention.

【図10】本発明の空気浄化膜の実施形態によるピリジ
ン浄化性能を示す説明図である。
FIG. 10 is an explanatory diagram showing pyridine purification performance according to an embodiment of the air purification membrane of the present invention.

【図11】本発明の空気浄化膜の乾燥状態におけるアセ
トアルデヒド吸着性能比較を示す説明図である。
FIG. 11 is an explanatory diagram showing a comparison of acetaldehyde adsorption performance in a dry state of the air purification membrane of the present invention.

【図12】従来の光触媒を用いた脱臭装置を示す構成図
である。
FIG. 12 is a configuration diagram showing a conventional deodorizing apparatus using a photocatalyst.

【符号の説明】[Explanation of symbols]

1 基材 2 下地膜 3 オーバーコート膜 4 吸着剤 5 光触媒 6 バインダー DESCRIPTION OF SYMBOLS 1 Base material 2 Undercoat film 3 Overcoat film 4 Adsorbent 5 Photocatalyst 6 Binder

Claims (5)

【特許請求の範囲】[Claims] 【請求項1】 吸着剤、もしくは、光触媒と吸着剤とを
含む下膜と、該下膜の表面を覆うと共に、該下膜より吸
着剤に対して光触媒を大く含む上膜とを備えることを特
徴とする空気浄化膜。
1. An adsorbent or a lower film containing a photocatalyst and an adsorbent, and an upper film covering the surface of the lower film and containing a photocatalyst larger than the lower film with respect to the adsorbent. An air purification membrane characterized by the following.
【請求項2】 上記上膜は、吸着剤と光触媒との重量比
が、1:9乃至1:49であることを特徴とする請求項
1に記載の空気浄化膜。
2. The air purification membrane according to claim 1, wherein the upper membrane has a weight ratio of the adsorbent to the photocatalyst of 1: 9 to 1:49.
【請求項3】 上記下膜と上記上膜との重量比は、1:
2乃至1:4であることを特徴とする請求項1に記載の
空気浄化膜。
3. The weight ratio of the lower film and the upper film is 1:
The air purification membrane according to claim 1, wherein the ratio is 2 to 1: 4.
【請求項4】 上記吸着剤として、ゼオライトを銅イオ
ン交換処理を施したものを用いることを特徴とする請求
項1に記載の空気浄化膜。
4. The air purification membrane according to claim 1, wherein the adsorbent is obtained by subjecting zeolite to a copper ion exchange treatment.
【請求項5】 吸着剤、もしくは、光触媒と吸着剤とを
含む塗液を基材に塗布し、加熱を行って下膜を形成し、 上記下膜表面に、該下膜より吸着剤に対して光触媒を大
く含む塗液を塗布した後、加熱を行って上膜を形成する
ことを特徴とする空気浄化膜の製造方法。
5. A coating solution containing an adsorbent or a photocatalyst and an adsorbent is applied to a substrate, and heated to form a lower film. On the surface of the lower film, the lower film reacts with the adsorbent. A method for producing an air purification film, which comprises applying a coating liquid containing a large amount of a photocatalyst and then heating to form an upper film.
JP8304274A 1996-11-15 1996-11-15 Air purifying film and its manufacture Pending JPH10137329A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8304274A JPH10137329A (en) 1996-11-15 1996-11-15 Air purifying film and its manufacture

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8304274A JPH10137329A (en) 1996-11-15 1996-11-15 Air purifying film and its manufacture

Publications (1)

Publication Number Publication Date
JPH10137329A true JPH10137329A (en) 1998-05-26

Family

ID=17931078

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8304274A Pending JPH10137329A (en) 1996-11-15 1996-11-15 Air purifying film and its manufacture

Country Status (1)

Country Link
JP (1) JPH10137329A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7247800B2 (en) * 1998-12-14 2007-07-24 Oki Electric Industry Co., Ltd. Module circuit board for semiconductor device having barriers to isolate I/O terminals from solder
JP2008208846A (en) * 2007-02-23 2008-09-11 Matsushita Electric Ind Co Ltd Heat insulating body

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0598185A (en) * 1991-10-03 1993-04-20 Matsushita Electric Ind Co Ltd Coating material
JPH07171408A (en) * 1993-06-28 1995-07-11 Ishihara Sangyo Kaisha Ltd Photocatalytic body and its production
JPH08141503A (en) * 1994-11-28 1996-06-04 Matsushita Electric Works Ltd Method for forming inorganic coating film
JPH08173512A (en) * 1994-12-27 1996-07-09 Sharp Corp Deodorizing element
JPH09227809A (en) * 1996-02-26 1997-09-02 Goyo Paper Working Co Ltd Liquid coloring material for coating material or the like, having deodorizing function
JPH1094587A (en) * 1996-09-24 1998-04-14 Sharp Corp Photocatalytic film

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0598185A (en) * 1991-10-03 1993-04-20 Matsushita Electric Ind Co Ltd Coating material
JPH07171408A (en) * 1993-06-28 1995-07-11 Ishihara Sangyo Kaisha Ltd Photocatalytic body and its production
JPH08141503A (en) * 1994-11-28 1996-06-04 Matsushita Electric Works Ltd Method for forming inorganic coating film
JPH08173512A (en) * 1994-12-27 1996-07-09 Sharp Corp Deodorizing element
JPH09227809A (en) * 1996-02-26 1997-09-02 Goyo Paper Working Co Ltd Liquid coloring material for coating material or the like, having deodorizing function
JPH1094587A (en) * 1996-09-24 1998-04-14 Sharp Corp Photocatalytic film

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7247800B2 (en) * 1998-12-14 2007-07-24 Oki Electric Industry Co., Ltd. Module circuit board for semiconductor device having barriers to isolate I/O terminals from solder
JP2008208846A (en) * 2007-02-23 2008-09-11 Matsushita Electric Ind Co Ltd Heat insulating body

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