JP2002071298A - Photocatalytic heat exchanger - Google Patents
Photocatalytic heat exchangerInfo
- Publication number
- JP2002071298A JP2002071298A JP2000260389A JP2000260389A JP2002071298A JP 2002071298 A JP2002071298 A JP 2002071298A JP 2000260389 A JP2000260389 A JP 2000260389A JP 2000260389 A JP2000260389 A JP 2000260389A JP 2002071298 A JP2002071298 A JP 2002071298A
- Authority
- JP
- Japan
- Prior art keywords
- heat exchanger
- photocatalyst
- photocatalytic
- present
- silica gel
- 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
- 230000001699 photocatalysis Effects 0.000 title claims abstract description 48
- 239000011941 photocatalyst Substances 0.000 claims abstract description 47
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 34
- 239000011230 binding agent Substances 0.000 claims abstract description 28
- 239000002245 particle Substances 0.000 claims description 26
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 18
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims description 18
- 229910002027 silica gel Inorganic materials 0.000 claims description 17
- 239000000741 silica gel Substances 0.000 claims description 17
- 239000003242 anti bacterial agent Substances 0.000 claims description 15
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical group [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 11
- 239000011248 coating agent Substances 0.000 claims description 11
- 238000000576 coating method Methods 0.000 claims description 11
- 229910052709 silver Inorganic materials 0.000 claims description 11
- 239000004332 silver Substances 0.000 claims description 11
- 229920000642 polymer Polymers 0.000 claims description 7
- 239000011148 porous material Substances 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 6
- 239000000919 ceramic Substances 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- 239000007769 metal material Substances 0.000 claims description 3
- 230000000844 anti-bacterial effect Effects 0.000 abstract description 12
- 230000001877 deodorizing effect Effects 0.000 abstract description 10
- 239000000377 silicon dioxide Substances 0.000 abstract description 8
- KHYMPNFZHMCNDP-VGMNWLOBSA-N OS(=O)(=O)ON1[C@H]2CN([C@@H](CC2)C2=NN=C(O2)[C@@H]2CCCN2)C1=O Chemical compound OS(=O)(=O)ON1[C@H]2CN([C@@H](CC2)C2=NN=C(O2)[C@@H]2CCCN2)C1=O KHYMPNFZHMCNDP-VGMNWLOBSA-N 0.000 abstract 1
- 229910052782 aluminium Inorganic materials 0.000 description 21
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 21
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 8
- 238000002474 experimental method Methods 0.000 description 7
- 239000004372 Polyvinyl alcohol Substances 0.000 description 6
- 229920002451 polyvinyl alcohol Polymers 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 241000588724 Escherichia coli Species 0.000 description 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 4
- 239000004568 cement Substances 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 239000001913 cellulose Substances 0.000 description 3
- 229920002678 cellulose Polymers 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 238000004332 deodorization Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000010419 fine particle Substances 0.000 description 2
- 230000001678 irradiating effect Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 229910000510 noble metal Inorganic materials 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 229920002689 polyvinyl acetate Polymers 0.000 description 2
- 239000011118 polyvinyl acetate Substances 0.000 description 2
- 239000003507 refrigerant Substances 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 2
- 235000019345 sodium thiosulphate Nutrition 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 229910021642 ultra pure water Inorganic materials 0.000 description 2
- 239000012498 ultrapure water Substances 0.000 description 2
- XHZPRMZZQOIPDS-UHFFFAOYSA-N 2-Methyl-2-[(1-oxo-2-propenyl)amino]-1-propanesulfonic acid Chemical compound OS(=O)(=O)CC(C)(C)NC(=O)C=C XHZPRMZZQOIPDS-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 102100024522 Bladder cancer-associated protein Human genes 0.000 description 1
- 101150110835 Blcap gene Proteins 0.000 description 1
- 102100032566 Carbonic anhydrase-related protein 10 Human genes 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 101000867836 Homo sapiens Carbonic anhydrase-related protein 10 Proteins 0.000 description 1
- 101100493740 Oryza sativa subsp. japonica BC10 gene Proteins 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical compound [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229920003145 methacrylic acid copolymer Polymers 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- 238000007146 photocatalysis Methods 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- CQLFBEKRDQMJLZ-UHFFFAOYSA-M silver acetate Chemical compound [Ag+].CC([O-])=O CQLFBEKRDQMJLZ-UHFFFAOYSA-M 0.000 description 1
- 229940071536 silver acetate Drugs 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F24—HEATING; RANGES; VENTILATING
- F24F—AIR-CONDITIONING; AIR-HUMIDIFICATION; VENTILATION; USE OF AIR CURRENTS FOR SCREENING
- F24F8/00—Treatment, e.g. purification, of air supplied to human living or working spaces otherwise than by heating, cooling, humidifying or drying
- F24F8/20—Treatment, e.g. purification, of air supplied to human living or working spaces otherwise than by heating, cooling, humidifying or drying by sterilisation
- F24F8/22—Treatment, e.g. purification, of air supplied to human living or working spaces otherwise than by heating, cooling, humidifying or drying by sterilisation using UV light
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明はエアコンの熱交換器
に関するものであり、家庭用および自動車用のエアコン
において、脱臭機能と熱交換器フィン上での細菌繁殖防
止を同時に実現する光触媒熱交換器に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a heat exchanger for an air conditioner, and more particularly to a photocatalytic heat exchanger for a home and automobile air conditioner, which simultaneously realizes a deodorizing function and prevention of bacterial growth on heat exchanger fins. About.
【0002】[0002]
【従来の技術】従来のエアコンにおける脱臭には、活性
炭、オゾン、貴金属系の酸化触媒などが用いられてき
た。しかしいずれの方法においても、エアコン本来の機
能である冷房や暖房の妨げにならないように、熱交換器
に出入りする空気の流路を妨げないような位置に設置す
る必要がある。そのため、臭気ガスとの接触面積が小さ
くなり、十分な脱臭性能が得られないのが現状である。2. Description of the Related Art Activated carbon, ozone, noble metal-based oxidation catalysts, and the like have been used for deodorization in conventional air conditioners. However, in either method, it is necessary to install the air conditioner at a position that does not obstruct the flow path of the air flowing into and out of the heat exchanger so as not to obstruct the cooling and heating functions inherent to the air conditioner. For this reason, the contact area with the odorous gas is small, and at present, sufficient deodorizing performance cannot be obtained.
【0003】上述した課題を解決する方法として、光触
媒である酸化チタン粉末をシリカ系無機バインダーとと
もに熱交換器のアルミフィン上に形成した構成の光触媒
熱交換器が提案されている(特開平8−296992号
公報)。具体的には、図4に示すように、アルミニウム
フィンの本体部41の表面に、耐食性被膜42と、酸化
チタン微粒子43およびシリカ系無機バインダー44か
ら成る被膜45とが順に形成され、酸化チタン微粒子4
3に紫外光を照射した際に、酸化チタン微粒子43の表
面で発生する光触媒作用により、接触した臭気ガスの分
解による脱臭が行われる。すなわち、臭気ガスとの接触
面積の大きな熱交換器に光触媒をコートした構成である
ため、従来の貴金属系の酸化触媒などを用いた脱臭方法
と比較して、優れた脱臭性能が得られる。As a method for solving the above-mentioned problem, there has been proposed a photocatalytic heat exchanger in which a titanium oxide powder as a photocatalyst is formed on an aluminum fin of a heat exchanger together with a silica-based inorganic binder (Japanese Patent Application Laid-Open No. Hei 8-8). No. 296992). Specifically, as shown in FIG. 4, a corrosion-resistant coating 42 and a coating 45 composed of titanium oxide fine particles 43 and a silica-based inorganic binder 44 are sequentially formed on the surface of the main body portion 41 of the aluminum fin. 4
By irradiating the ultraviolet light 3 with the ultraviolet light, deodorization is performed by decomposition of the odor gas contacted by the photocatalytic action generated on the surface of the titanium oxide fine particles 43. That is, since the heat exchanger having a large contact area with the odor gas is coated with the photocatalyst, excellent deodorizing performance can be obtained as compared with a conventional deodorizing method using a noble metal-based oxidation catalyst or the like.
【0004】さらに、酸化チタンの光触媒作用には抗菌
効果もあるため、上述した構成の光触媒熱交換器は、脱
臭性と親水性に加えて抗菌性能も併せ持つといった特徴
を有する。Further, since the photocatalytic action of titanium oxide also has an antibacterial effect, the photocatalytic heat exchanger having the above-mentioned structure has a feature that it has antibacterial performance in addition to deodorization and hydrophilicity.
【0005】[0005]
【発明が解決しようとする課題】しかしながら、上記光
触媒熱交換器においては、アルミフィン表面における光
触媒作用は、紫外ランプが照射されている時のみ出現す
る効果である。すなわち、ランプによる紫外光が当たら
ない、または当たりにくい領域にあるアルミフィン表面
において、細菌が繁殖することを防ぐことができないと
言った欠点がある。さらに、バインダーにシリカ系無機
物を用いているため、冷暖運転の開始直後に、不快なセ
メント臭が発生する。この問題を解決するには、有機系
バインダーを用いることが有効である。しかし、有機系
バインダーを用いると、酸化チタンの光触媒作用で、接
触した臭気ガスを分解するだけでなく、有機系バインダ
ーも分解してしまうため、紫外ランプを照射して長時間
使用すると酸化チタン粉末が剥離してしまうといった課
題もあった。However, in the above-described photocatalytic heat exchanger, the photocatalytic action on the surface of the aluminum fin is an effect that appears only when the ultraviolet lamp is irradiated. That is, there is a defect that bacteria cannot be prevented from growing on the surface of the aluminum fin that is not or hardly hit by ultraviolet light from the lamp. Furthermore, since a silica-based inorganic substance is used for the binder, an unpleasant cement odor is generated immediately after the start of the cooling / heating operation. In order to solve this problem, it is effective to use an organic binder. However, when an organic binder is used, the photocatalytic action of titanium oxide not only decomposes the odorous gas that has come into contact, but also decomposes the organic binder. However, there is also a problem that the particles are peeled off.
【0006】本発明は、このような従来の問題点を解決
するものであり、家庭用や自動車用などのエアコンにお
いて優れた脱臭機能に加えて抗菌性能を有した光触媒熱
交換器を提供することを目的とする。An object of the present invention is to provide a photocatalyst heat exchanger having an antibacterial performance in addition to an excellent deodorizing function in an air conditioner for home use or automobile use. With the goal.
【0007】[0007]
【課題を解決するための手段】上記目的を達成するため
に本発明の光触媒熱交換器は、熱伝導性金属材料から成
るフィン表面を、光触媒と無機系抗菌剤と有機系バイン
ダーで被覆した構成であることを特徴とする。In order to achieve the above object, a photocatalyst heat exchanger according to the present invention comprises a fin surface made of a heat conductive metal material coated with a photocatalyst, an inorganic antibacterial agent and an organic binder. It is characterized by being.
【0008】上記の如く、光触媒に加えて無機系抗菌剤
も有機系バインダーとともにフィン表面上に被覆した構
成としたことにより、光の当たりにくいフィン表面にお
いても優れた抗菌性能を有することができる。また、有
機系バインダーを用いるため、シリカ系無機バインダー
を用いた場合の不快なセメント臭の発生をなくすことが
できる。As described above, in addition to the photocatalyst, an inorganic antibacterial agent is coated on the fin surface together with the organic binder, so that excellent antibacterial performance can be obtained even on the fin surface where light is hardly exposed. Moreover, since an organic binder is used, it is possible to eliminate the generation of unpleasant cement odor when a silica-based inorganic binder is used.
【0009】請求項2の発明は、請求項1の発明のおけ
る光触媒に酸化チタン粒子の表面に微細な細孔を有する
光触媒として不活性なセラミック膜をコートした光触媒
粒子を用いることを特徴としている。ことにより、酸化
チタンと有機系バインダーが直接接触することがなくな
るため、紫外光照射時の酸化チタンの光触媒作用によ
り、有機系バインダーが分解・劣化することを防ぐこと
ができる。A second aspect of the present invention is characterized in that the photocatalyst according to the first aspect of the present invention uses, as the photocatalyst having fine pores on the surface of titanium oxide particles, a photocatalytic particle coated with an inert ceramic film. . This prevents direct contact between the titanium oxide and the organic binder, so that the organic binder can be prevented from decomposing and deteriorating due to the photocatalytic action of the titanium oxide during ultraviolet light irradiation.
【0010】ここで、熱伝導性金属材料は、アルミニウ
ムまたはアルミニウム合金であることが望ましい。Here, the heat conductive metal material is preferably aluminum or an aluminum alloy.
【0011】また、請求項3の発明は、請求項1の発明
において、上記有機系バインダーが親水性を有する高分
子化合物であることを特徴とする。バインダーが親水性
を有する構成としたのは、用いる光触媒粒子が、酸化チ
タン粒子の表面に微細な細孔を有する光触媒として不活
性なセラミック膜をコートした構造であるため、従来の
酸化チタン粉末を用いた場合と比較して、光触媒粒子表
面での超親水性の効果が低下してしまうことを、バイン
ダーの親水性で補うためである。The invention of claim 3 is characterized in that, in the invention of claim 1, the organic binder is a polymer compound having hydrophilicity. The binder has a hydrophilic structure because the photocatalyst particles used have a structure in which the surface of the titanium oxide particles is coated with an inert ceramic film as a photocatalyst having fine pores. This is because the decrease in the superhydrophilicity effect on the surface of the photocatalyst particles as compared with the case where it is used is compensated for by the hydrophilicity of the binder.
【0012】このとき、親水性を有する高分子化合物と
しては、(メタ)アクリル酸またはビニルアルコールを
重合単位として含む重合体、セルロース系化合物もしく
はそれらの混合物であることが望ましい。At this time, the polymer compound having hydrophilicity is preferably a polymer containing (meth) acrylic acid or vinyl alcohol as a polymerized unit, a cellulose compound, or a mixture thereof.
【0013】また、請求項3は、請求項1において、無
機系抗菌剤が、シリカゲルにチオスルファト銀錯体を担
持させかつ前記シリカゲルの表面の少なくとも一部をテ
トラアルコキシシランの加水分解物で被覆してなる銀シ
リカゲル系抗菌剤であることを特徴としている。According to a third aspect of the present invention, in the first aspect, the inorganic antibacterial agent comprises a silica gel carrying a thiosulfatosilver complex and at least a part of the surface of the silica gel coated with a hydrolyzate of tetraalkoxysilane. Silver silica gel antibacterial agent.
【0014】[0014]
【発明の実施の形態】本発明の一形態を、図1〜図3に
基づいて、以下に説明する。図1は本発明の光触媒熱交
換器を用いたエアコンの室内ユニット内部の側面概略
図、図2は本発明の光触媒熱交換器の斜視図、図3は本
発明の光触媒熱交換器のアルミニウムフィンの断面図で
ある。DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS One embodiment of the present invention will be described below with reference to FIGS. 1 is a schematic side view of the inside of an indoor unit of an air conditioner using the photocatalytic heat exchanger of the present invention, FIG. 2 is a perspective view of the photocatalytic heat exchanger of the present invention, and FIG. 3 is an aluminum fin of the photocatalytic heat exchanger of the present invention. FIG.
【0015】図1に示すように、室内ユニット11内に
は、光触媒熱交換器12と、紫外線ランプ(15W;ピ
ーク波長365nm)13と、送風機14とが設けられ
ている。上記光触媒熱交換器12は、図2に示すよう
に、冷媒の通路である金属製パイプ22にアルミニウム
フィン21が一定間隔を置いて平行に多数取り付けられ
た構造である。また、図3に示すように、上記アルミニ
ウムフィン21は、アルミニウムから成る本体部31の
表面に、酸化チタン粒子の表面に微細な細孔を有する光
触媒として不活性なセラミック膜をコートした光触媒粒
子32と、チオスルファト銀錯体を含む銀シリカゲル系
抗菌剤粒子33、および有機系バインダー34からなる
被膜35が形成された構造である。As shown in FIG. 1, a photocatalytic heat exchanger 12, an ultraviolet lamp (15 W; peak wavelength 365 nm) 13, and a blower 14 are provided in the indoor unit 11. As shown in FIG. 2, the photocatalyst heat exchanger 12 has a structure in which a large number of aluminum fins 21 are attached in parallel at regular intervals to a metal pipe 22 which is a passage for a refrigerant. As shown in FIG. 3, the aluminum fins 21 are made of a photocatalyst particle 32 formed by coating a surface of a main body 31 made of aluminum with an inert ceramic film as a photocatalyst having fine pores on the surface of titanium oxide particles. And a coating 35 composed of silver silica gel-based antibacterial agent particles 33 containing a thiosulfatosilver complex and an organic binder 34.
【0016】ここで、上記室内ユニット11において、
室内の空気は矢印に示したように、室内ユニット11の
上部から光触媒熱交換器12を通り、さらに送風機14
を通った後、室内ユニット11の下部から室内に吐出さ
れる。また、紫外線ランプ13を点灯させておくことに
より、光触媒熱交換器12のアルミニウムフィン21表
面に形成した被膜25内の光触媒粒子23に接触した室
内の空気に含まれる臭気ガスが、光触媒作用により分解
され脱臭が行われる。更に、有機系バインダー34は親
水性を有するため、アルミニウムフィン21表面に水滴
が生成し、そのまま風にのって吹き出し口より室内に吹
き出し床を濡らすという問題が発生するのを阻止でき
る。Here, in the indoor unit 11,
As shown by the arrow, the indoor air passes through the photocatalytic heat exchanger 12 from above the indoor unit 11 and further passes through the blower 14.
After passing through, the air is discharged from the lower part of the indoor unit 11 into the room. Further, by turning on the ultraviolet lamp 13, the odor gas contained in the room air in contact with the photocatalyst particles 23 in the coating 25 formed on the surface of the aluminum fin 21 of the photocatalyst heat exchanger 12 is decomposed by photocatalysis. It is deodorized. Further, since the organic binder 34 has hydrophilicity, it is possible to prevent water droplets from being formed on the surface of the aluminum fins 21 and to prevent the problem that the floor is blown into the room from the blow-out opening and the floor is wet.
【0017】[0017]
【実施例】以下、本発明の光触媒熱交換器についてその
製造方法とともに説明する。DESCRIPTION OF THE PREFERRED EMBODIMENTS The photocatalyst heat exchanger of the present invention will be described below together with its manufacturing method.
【0018】(実施例)アルミニウムフィン材料とし
て、あらかじめ脱脂および水洗したアルミニウム板(材
質:1330、厚さ0.1mm、質別:H26)を用い
た。また光触媒粉末には、粒径約40nmのアナターゼ
型酸化チタン粒子の表面を、10nmの細孔をもつ多孔
質アルミナでコートした粉末(例えば、特許公報:第2
945926号)を用い、バインダーには、親水性を有
する高分子化合物であるポリビニルアルコールを用い
た。また、無機系抗菌剤には銀シリカゲル系抗菌剤粒子
(粒径約0.4μm)を用いた。(Example) As an aluminum fin material, an aluminum plate (material: 1330, thickness: 0.1 mm, temper: H26) which had been degreased and washed in advance was used. The photocatalyst powder is a powder obtained by coating the surface of anatase-type titanium oxide particles having a particle size of about 40 nm with porous alumina having pores of 10 nm (for example, Patent Publication: No. 2).
No. 945926), and polyvinyl alcohol, which is a polymer compound having hydrophilicity, was used as the binder. In addition, silver silica gel antibacterial particles (particle diameter: about 0.4 μm) were used as the inorganic antibacterial agent.
【0019】ここで、銀シリカゲル系抗菌剤の製造方法
を説明する。酢酸銀などの水溶性銀塩100重量部を塩
素を含まない水に加えて溶解させ、亜硫酸ナトリウムお
よび亜硫酸水素ナトリウムの混合物450重量部と、チ
オ硫酸ナトリウム塩300重量部とを順次かつ攪拌しな
がら混合し溶解させ、銀錯体水溶液を得る。チオ硫酸ナ
トリウムの重量は、その水和物Na2S2O3・5H2Oの重量と
して示される。次に、平均粒径3μmのシリカゲル粉末
を180℃で2時間以上乾燥させたもの100重量部に対
し、銀成分として2重量部になるように前記チオスルフ
ァト銀錯体水溶液に混合する。ついで、速やかに溶媒お
よびシリカゲル中に吸収された水分を除去する。これを
所定の粒径(約0.4μm)に粉砕することにより、抗
菌材料を担持したシリカゲルを得る。コーティング材料
として、テトラエトキシシラン100重量部をエチルア
ルコール100重量部に希釈混合させた溶液に、上記抗
菌材料担持シリカゲル100重量部を分散させ、上記シ
リカゲルの表面の少なくとも一部をコーティングする。
ついでこれを乾燥させ、銀シリカゲル系抗菌剤を得る。Here, a method for producing the silver silica gel antibacterial agent will be described. 100 parts by weight of a water-soluble silver salt such as silver acetate is added to and dissolved in water containing no chlorine, and 450 parts by weight of a mixture of sodium sulfite and sodium bisulfite and 300 parts by weight of sodium thiosulfate are sequentially and stirred. Mix and dissolve to obtain an aqueous silver complex solution. The weight of sodium thiosulfate is given as the weight of its hydrate, Na 2 S 2 O 3 .5H 2 O. Next, 100 parts by weight of a silica gel powder having an average particle size of 3 μm dried at 180 ° C. for 2 hours or more are mixed with the above-mentioned aqueous solution of silver thiosulfato complex so as to become 2 parts by weight as a silver component. Next, the solvent and the water absorbed in the silica gel are promptly removed. This is pulverized to a predetermined particle size (about 0.4 μm) to obtain silica gel carrying an antibacterial material. As a coating material, 100 parts by weight of the antibacterial material-supporting silica gel is dispersed in a solution obtained by diluting 100 parts by weight of tetraethoxysilane with 100 parts by weight of ethyl alcohol, and at least a part of the surface of the silica gel is coated.
Then, this is dried to obtain a silver silica gel antibacterial agent.
【0020】上述した、多孔質アルミナでコートした酸
化チタン光触媒粉末と銀シリカゲル系抗菌剤を、親水性
を有する有機系バインダーとしてのポリビニルアルコー
ルとともに、アルミニウムフィン上に塗布し、200℃
で30秒間加熱乾燥させ、アルミニウムフィン上に厚さ
1μmの光触媒皮膜を形成した。そして、揮発性プレス
油を用いて上記フィン材料をプレス加工し、所定の形状
のフィンを形成した。さらに、このフィンを冷媒用チュ
ーブに組み合わせた後、所定の温度で加熱乾燥すること
により、揮発性プレス油を脱脂し、光触媒熱交換器Aを
作製した。The above-mentioned titanium oxide photocatalyst powder coated with porous alumina and a silver silica gel antibacterial agent are applied on aluminum fins together with a polyvinyl alcohol as a hydrophilic organic binder at 200 ° C.
For 30 seconds to form a photocatalytic film having a thickness of 1 μm on the aluminum fins. Then, the fin material was pressed using a volatile press oil to form fins having a predetermined shape. Further, after assembling the fins with a tube for a refrigerant, the pressurized press oil was degreased by heating and drying at a predetermined temperature to produce a photocatalyst heat exchanger A.
【0021】(比較例)次に、比較例として、光触媒粉
末に粒径約7nmのアナターゼ型酸化チタン粒子(石原
産業:ST−01)を、バインダーにはシリカ系無機物
を用い、アルミニウムフィン上に塗布した後150℃で
30分間加熱乾燥させ、厚さ1μmの光触媒被膜を形成
した。そして、上述した方法と同様に光触媒熱交換器B
を作製した。Comparative Example Next, as a comparative example, anatase-type titanium oxide particles (ST-01, Ishihara Sangyo) having a particle size of about 7 nm were used as a photocatalyst powder, and a silica-based inorganic material was used as a binder. After the application, it was dried by heating at 150 ° C. for 30 minutes to form a photocatalytic film having a thickness of 1 μm. Then, similarly to the above-described method, the photocatalytic heat exchanger B
Was prepared.
【0022】(実験1)上記本発明の光触媒熱交換器A
および比較例の光触媒熱交換器Bのフィンの一部を切り
出して(サイズ10mm×10mm)、各試料を作製し
た後、これら試料における抗菌性の評価を行った。具体
的な評価方法は、滅菌したガラスシャーレを3個準備
し、それぞれのシャーレにアルコールで十分に洗浄した
各試料を入れて、湿度90%で温度35℃に保持した恒
温糟に入れ、大腸菌を同量(約1×105個/ml)ず
つ、上記各試料上に滴下して18時間保持した後、各試
料上の大腸菌の量を測定することによって行った。な
お、上記恒温糟中には、5Wの蛍光灯が設置してあり、
シャーレ中の試料に光が照射されるようになっている。(Experiment 1) The photocatalyst heat exchanger A of the present invention described above.
A part of the fins of the photocatalyst heat exchanger B of the comparative example was cut out (size: 10 mm × 10 mm), and after preparing each sample, the antibacterial properties of these samples were evaluated. A specific evaluation method is to prepare three sterilized glass Petri dishes, put each sample thoroughly washed with alcohol in each Petri dish, put them in a constant temperature bath maintained at a temperature of 35% at a humidity of 90%, and remove E. coli. The same amount (approximately 1 × 10 5 cells / ml) was dropped on each of the above samples and kept for 18 hours, and then the amount of E. coli on each sample was measured. In addition, a 5W fluorescent lamp is installed in the above constant temperature vessel,
The sample in the petri dish is irradiated with light.
【0023】その結果、蛍光灯の照射を行った場合に
は、比較の光触媒熱交換器Bでは大腸菌数が約約1×1
03個/mlまでしか減少していないのに対して、本発
明の光触媒熱交換器Aでは約100個まで減少している
ことが認められた。また、蛍光灯の照射を行わない場合
には、比較の光触媒熱交換器Bでは大腸菌数が約9×1
04個/mlまでしか減少しないのに対し、本発明の光
触媒熱交換器Aでは約5×102個/mlまで減少して
いることが認められた。As a result, when irradiation with a fluorescent lamp was performed, the number of E. coli in the comparative photocatalytic heat exchanger B was about 1 × 1.
0 whereas only up to 3 cells / ml not reduced, it was found that reduced to about 100 in the photocatalyst heat exchanger A of the present invention. When the fluorescent lamp was not irradiated, the number of E. coli in the comparative photocatalytic heat exchanger B was about 9 × 1.
0 up to 4 / ml while only decreased and it is observed that is reduced to about 5 × 10 2 cells / ml in photocatalytic heat exchanger A of the present invention.
【0024】このように、本発明の光触媒熱交換器は、
特に光の照射がない場合においても優れた抗菌性能を有
していた。As described above, the photocatalytic heat exchanger of the present invention
In particular, it had excellent antibacterial performance even without light irradiation.
【0025】(実験2)得られた光触媒熱交換器Aおよ
び光触媒熱交換器Bについて、臭気の評価を行った。臭
気評価は、パネラーにより、息を吹きかけた後の官能評
価を行った。その結果、従来の光触媒熱交換器Bにはか
なり強い臭気が感じられたのに対し、本発明の光触媒熱
交換器Aにはほとんど感じられなかった。(Experiment 2) The obtained photocatalytic heat exchanger A and photocatalytic heat exchanger B were evaluated for odor. The odor was evaluated by a panelist after performing a breath blow. As a result, the photocatalyst heat exchanger B of the present invention felt a rather strong odor, while the photocatalyst heat exchanger A of the present invention hardly felt it.
【0026】(実験3)次に、上記本発明の光触媒熱交
換器Aを用いたエアコンの室内機及び上記比較例の光触
媒熱交換器Bを用いて、エアコンの室内機(共に、図1
に示す構造のもの)による脱臭性能の評価を行った。具
体的な評価方法は、光触媒熱交換器Aおよび光触媒熱交
換器Bを用いたエアコンの室内機、それぞれ、高さ2
m、幅4m、奥行4mの大きさで室温28℃の気密実験
室(15ppmの濃度のアセトアルデヒドを充填)内に
設置して、温度を20℃に設定し、湿度を40%に保持
しつつ冷房運転を行い、アセトアルデヒドの光触媒分解
性能を測定することにより行った。なお、通常室外の出
す除湿の結露水のドレインは、実験室の気密を確実にす
るために、気密実験室内にもうけたポリタンク内にドレ
インのホースを導いた。(Experiment 3) Next, the indoor unit of an air conditioner using the photocatalytic heat exchanger A of the present invention and the indoor unit of the air conditioner using the photocatalytic heat exchanger B of the comparative example (both in FIG. 1)
The deodorizing performance was evaluated by the following structure. The specific evaluation method is as follows: an indoor unit of an air conditioner using the photocatalyst heat exchanger A and the photocatalyst heat exchanger B;
m, width 4 m, depth 4 m, placed in an airtight laboratory (filled with 15 ppm concentration of acetaldehyde) at room temperature 28 ° C., set the temperature at 20 ° C., and keep the humidity at 40% while cooling. The operation was performed, and the photocatalytic decomposition performance of acetaldehyde was measured. In addition, the drain hose of the dehumidified dew condensation water which is usually taken out of the room was guided into a plastic tank provided in the airtight laboratory in order to ensure the airtightness of the laboratory.
【0027】その結果、比較の光触媒熱交換器Bを用い
たエアコンの室内機では、約30分後のアセトアルデヒ
ドの濃度は8ppm、1時間後に3ppmであった。本
発明の光触媒熱交換器Aは、約30分後のアセトアルデ
ヒドの濃度は8ppmであり、1時間後に3ppmであ
った。すなわち、本発明の光触媒熱交換器Aは、従来の
光触媒熱交換器Bと同じように優れた脱臭性を有するこ
とがわかった。As a result, in the indoor unit of the air conditioner using the comparative photocatalytic heat exchanger B, the concentration of acetaldehyde after about 30 minutes was 8 ppm, and 3 ppm after 1 hour. In the photocatalyst heat exchanger A of the present invention, the concentration of acetaldehyde after about 30 minutes was 8 ppm, and was 3 ppm after 1 hour. That is, it was found that the photocatalyst heat exchanger A of the present invention had excellent deodorizing properties as in the case of the conventional photocatalyst heat exchanger B.
【0028】(実験4)また、得られた光触媒熱交換器
Aおよび光触媒熱交換器Bについて、フィンの一部を切
り出して(サイズ:5mm角)、各試料を作製した後、
これら試料の水滴の接触角を測定することにより、親水
性の評価を行った。なお、親水性の評価は、紫外線領域
の蛍光灯光源(15W;ピーク波長365nm)を用い
て、照射距離25cmで各試料を10分間照射した後、
一定時間経過ごとに、各試料の平滑な表面の上部にマイ
クロシリンダを用いて超純水1マイクロリットル(μ
l)を滴下し、超純水の接触角を接触角計を用いて測定
するというものである。(Experiment 4) Further, with respect to the obtained photocatalyst heat exchanger A and photocatalyst heat exchanger B, a part of the fin was cut out (size: 5 mm square) to prepare each sample.
The hydrophilicity was evaluated by measuring the contact angles of water drops of these samples. The hydrophilicity was evaluated by irradiating each sample for 10 minutes at an irradiation distance of 25 cm using a fluorescent lamp light source (15 W; peak wavelength 365 nm) in the ultraviolet region.
After a certain period of time, 1 microliter of ultrapure water (μ
1) is dropped, and the contact angle of ultrapure water is measured using a contact angle meter.
【0029】その結果、本発明の光触媒熱交換器Aにお
けるフィンの接触角は経過時間測定開始の直後が8゜で
あり、12時間後が11゜、36時間後でも12゜であ
った。また、比較の光触媒熱交換器Bにおけるフィンの
接触角は経過時間測定開始の直後が7゜であり、12時
間後が12゜、36時間後には14゜であった。As a result, the contact angle of the fins in the photocatalytic heat exchanger A of the present invention was 8 ° immediately after the start of elapsed time measurement, 11 ° after 12 hours, and 12 ° after 36 hours. The contact angle of the fins in the comparative photocatalytic heat exchanger B was 7 ° immediately after the start of the elapsed time measurement, 12 ° after 12 hours, and 14 ° after 36 hours.
【0030】以上の結果から、本発明の光触媒熱交換A
は、従来の光触媒熱交換器Bと同程度の親水性を有して
いることがわかった。From the above results, the photocatalytic heat exchange A of the present invention
Was found to have the same level of hydrophilicity as the conventional photocatalytic heat exchanger B.
【0031】以上の実験1のおよび実験2の結果から、
本発明の光触媒熱交換器Aは、従来の光触媒熱交換器B
と比較して、優れた抗菌性能を有し、従来の光触媒熱交
換器の有するセメント臭の課題を解決するものであろこ
とがわかる。また実験3および実験4の結果から、従来
の光触媒熱交換器と同等な脱臭性能および親水特性を有
していることがわかる。From the results of Experiment 1 and Experiment 2,
The photocatalyst heat exchanger A of the present invention is different from the conventional photocatalyst heat exchanger B
It can be seen that it has excellent antibacterial performance and solves the problem of cement odor of the conventional photocatalytic heat exchanger as compared with the conventional method. In addition, the results of Experiments 3 and 4 show that they have the same deodorizing performance and hydrophilic properties as those of the conventional photocatalytic heat exchanger.
【0032】なお、本発明の実施例の光触媒粒子におい
て、酸化チタン粒子の表面にコートする微細な細孔を有
する光触媒不活性なセラミック膜としてアルミナを用い
たが、これに限るものではなく、アモルファスの酸化チ
タン、酸化ジルコニウム、酸化シリコン、酸化マグネウ
ム、酸化カルシウムでも同様の結果が得られた。In the photocatalyst particles of the embodiment of the present invention, alumina was used as the photocatalytically inactive ceramic film having fine pores coated on the surface of the titanium oxide particles. However, the present invention is not limited to this. Similar results were obtained with titanium oxide, zirconium oxide, silicon oxide, magnesium oxide and calcium oxide.
【0033】なお、本発明の実施例における有機系バイ
ンダーにポリビニルアルコールを用いたが、これに限る
ものではなく、(メタ)アクリル酸またはビニルアルコ
ールを重合単位として含む重合体、セルロース系化合物
もしくはそれらの混合物であれば同様の結果が得られ
た。具体的には、ポリ(メタ)アクリル酸、ポリ(メ
タ)アクリル酸とポリ酢酸ビニルとの共重合体、ポリ
(メタ)アクリル酸とポリビニルアルコールとの共重合
体、ポリ(メタ)アクリル酸とセルロースの共重合体、
ポリ(メタ)アクリル酸とデンプンとの共重合体、ポリ
(メタ)アクリルアミド、ポリ(メタ)アクリルアミド
メチルプロパンスルホン酸、(メタ)アクリル酸とポリ
アミドとの共重合体、ポリビニルアルコール、ポリ酢酸
ビニルの部分ケン化物、セルロース系樹脂である。In the examples of the present invention, polyvinyl alcohol was used as the organic binder. However, the present invention is not limited to this. For example, a polymer containing (meth) acrylic acid or vinyl alcohol as a polymerization unit, a cellulose compound, or a polymer thereof may be used. In the case of a mixture of the above, similar results were obtained. Specifically, poly (meth) acrylic acid, a copolymer of poly (meth) acrylic acid and polyvinyl acetate, a copolymer of poly (meth) acrylic acid and polyvinyl alcohol, and poly (meth) acrylic acid Cellulose copolymer,
Copolymer of poly (meth) acrylic acid and starch, poly (meth) acrylamide, poly (meth) acrylamidomethylpropanesulfonic acid, copolymer of (meth) acrylic acid and polyamide, polyvinyl alcohol, polyvinyl acetate It is a partially saponified product and a cellulosic resin.
【0034】なお、本発明の実施例において、アルミニ
ウムなどのフィン上に直接光触媒皮膜を形成した構成と
したが、これに限るものではなく、アルミニウムフィン
上に耐食性皮膜としてクロメート処理層を設け、その上
に光触媒皮膜を形成した構成においても同様の効果が得
られた。In the embodiment of the present invention, the photocatalyst film is formed directly on the fins of aluminum or the like. However, the present invention is not limited to this. A chromate treatment layer is provided on the aluminum fins as a corrosion-resistant film. The same effect was obtained in the configuration in which the photocatalytic film was formed thereon.
【0035】[0035]
【発明の効果】以上の説明から明らかなように、本発明
の光触媒熱交換器は、熱交換器のフィン表面を光触媒と
無機系抗菌剤と有機系バインダーで被覆した構成である
ため、従来の酸化チタン粒子とシリカ系無機バインダー
で被覆した場合と比較して、優れた脱臭性能および親水
性能を有するだけでなく、セメント臭の発生がなく、さ
らに優れた抗菌性能を有するといった効果を奏する。As is apparent from the above description, the photocatalyst heat exchanger of the present invention has a structure in which the fin surface of the heat exchanger is coated with a photocatalyst, an inorganic antibacterial agent and an organic binder. As compared with the case where the titanium oxide particles are coated with the silica-based inorganic binder, not only are excellent deodorizing performance and hydrophilic performance, but also no generation of cement odor, and further excellent antibacterial performance.
【図1】本発明の光触媒熱交換器を用いたエアコンの室
内ユニット内部の側面概略図FIG. 1 is a schematic side view of the interior of an indoor unit of an air conditioner using the photocatalytic heat exchanger of the present invention.
【図2】本発明の光触媒熱交換器の斜視図FIG. 2 is a perspective view of the photocatalytic heat exchanger of the present invention.
【図3】本発明のアルミニウムフィンの断面図FIG. 3 is a cross-sectional view of the aluminum fin of the present invention.
【図4】従来の光触媒熱交換器の断面図FIG. 4 is a cross-sectional view of a conventional photocatalytic heat exchanger.
11 エアコンの室内機ユニット 12 光触媒熱交換器 13 紫外線ランプ 14 送風機 21 光触媒被膜を形成したアルミニウムフィン 22 金属性パイプ 31 アルミニウムフィン 32 表面を微細な細孔を有する光触媒として不活性な
アルミナ膜をコートした光触媒粒子 33 無機系抗菌剤(銀シリカゲル系抗菌剤粒子) 34 有機系バインダー(ポリビニルアルコール) 35 光触媒被膜 41 アルミニウムフィン 42 酸化チタン粒子 43 シリカ系無機バインダー 44 光触媒被膜Reference Signs List 11 Indoor unit of air conditioner 12 Photocatalytic heat exchanger 13 Ultraviolet lamp 14 Blower 21 Aluminum fin with photocatalytic coating 22 Metallic pipe 31 Aluminum fin 32 The surface was coated with an inert alumina film as a photocatalyst having fine pores Photocatalyst particles 33 Inorganic antibacterial agent (silver silica gel antibacterial agent particles) 34 Organic binder (polyvinyl alcohol) 35 Photocatalytic coating 41 Aluminum fin 42 Titanium oxide particles 43 Silica-based inorganic binder 44 Photocatalytic coating
フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) B01J 37/02 301 F25B 39/00 P F24F 1/00 F28F 13/18 B F25B 39/00 B01D 53/36 H F28F 13/18 F24F 1/00 371Z (72)発明者 冨岡 敏一 大阪府門真市大字門真1006番地 松下電器 産業株式会社内 Fターム(参考) 3L051 BC03 BC05 BC10 4C080 AA07 AA10 BB02 BB05 CC01 HH05 JJ04 KK08 LL10 MM02 QQ17 4D048 AA22 AB01 AB03 BA03X BA07X BB03 BC07 CC33 CC34 CC42 EA01 4G069 AA03 AA08 AA09 BA01B BA04A BA04B BA04C BA17 BA48A BA48C CA01 CA07 CA10 CA17 DA06 EC22Y EE01 EE07 FA04 FB23 Continued on the front page (51) Int.Cl. 7 Identification symbol FI Theme coat II (reference) B01J 37/02 301 F25B 39/00 P F24F 1/00 F28F 13/18 B F25B 39/00 B01D 53/36 H F28F 13 / 18 F24F 1/00 371Z (72) Inventor Toshioka Toshioka 1006 Kazuma, Kazuma, Osaka Prefecture Matsushita Electric Industrial Co., Ltd. F-term (reference) 3L051 BC03 BC05 BC10 4C080 AA07 AA10 BB02 BB05 CC01 HH05 JJ04 KK08 LL10 MM02Q17 4D048 AA22 AB01 AB03 BA03X BA07X BB03 BC07 CC33 CC34 CC42 EA01 4G069 AA03 AA08 AA09 BA01B BA04A BA04B BA04C BA17 BA48A BA48C CA01 CA07 CA10 CA17 DA06 EC22Y EE01 EE07 FA04 FB23
Claims (4)
が、光触媒と無機系抗菌剤と有機系バインダーで被覆し
た構成であることを特徴とする光触媒熱交換器。1. A photocatalytic heat exchanger, wherein a fin surface made of a heat conductive metal material is coated with a photocatalyst, an inorganic antibacterial agent and an organic binder.
な細孔を有する光触媒として不活性なセラミック膜をコ
ートした構成の粒子である請求項1記載の光触媒熱交換
器。2. The photocatalyst heat exchanger according to claim 1, wherein the photocatalyst is a particle in which titanium oxide particles are coated with an inert ceramic film as a photocatalyst having fine pores on the surface.
子化合物である請求項1記載の光触媒熱交換器。3. The photocatalytic heat exchanger according to claim 1, wherein the organic binder is a polymer compound having hydrophilicity.
ファト銀錯体を担持させかつ前記シリカゲルの表面の少
なくとも一部をテトラアルコキシシランの加水分解物で
被覆してなる銀シリカゲル系抗菌剤であることを特徴と
する請求項1記載の光触媒熱交換器。4. The method according to claim 1, wherein the inorganic antibacterial agent is a silver silica gel antibacterial agent obtained by supporting a thiosulfatosilver complex on silica gel and coating at least a part of the surface of the silica gel with a hydrolyzate of tetraalkoxysilane. The photocatalyst heat exchanger according to claim 1, characterized in that:
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JP2000260389A JP2002071298A (en) | 2000-08-30 | 2000-08-30 | Photocatalytic heat exchanger |
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JP2000260389A JP2002071298A (en) | 2000-08-30 | 2000-08-30 | Photocatalytic heat exchanger |
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Family
ID=18748408
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Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004184023A (en) * | 2002-12-05 | 2004-07-02 | Shin Nippon Air Technol Co Ltd | Air-conditioning equipment subjected to antibacterial treatment |
WO2005026276A1 (en) * | 2003-09-11 | 2005-03-24 | Kabushiki Kaisha Zac | Coating material |
JP2005254085A (en) * | 2004-03-10 | 2005-09-22 | Daicel Chem Ind Ltd | Surface-modified titanium oxide photocatalyst and method of oxidizing organic compound using it |
WO2008132807A1 (en) * | 2007-04-20 | 2008-11-06 | Panasonic Corporation | Air cleaner, and air conditioner or refrigerator using the air cleaner |
JP2009150585A (en) * | 2007-12-19 | 2009-07-09 | Sumitomo Light Metal Ind Ltd | Fin material for heat exchanger and its manufacturing method |
JP2012522965A (en) * | 2009-04-02 | 2012-09-27 | ヘンケル・アクチェンゲゼルシャフト・ウント・コムパニー・コマンディットゲゼルシャフト・アウフ・アクチェン | Automotive heat exchanger parts coated with ceramic |
JP2019116991A (en) * | 2017-12-27 | 2019-07-18 | 株式会社中部テクノ | Sterilizer of refrigeration mechanism |
KR20190128946A (en) * | 2018-05-09 | 2019-11-19 | 엘지전자 주식회사 | Coating layer |
KR20210115583A (en) * | 2020-03-13 | 2021-09-27 | 오충록 | Photocatalytic Paint Composition for Ventilator and Filter Box and Manufacturing Method of thereof |
-
2000
- 2000-08-30 JP JP2000260389A patent/JP2002071298A/en active Pending
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004184023A (en) * | 2002-12-05 | 2004-07-02 | Shin Nippon Air Technol Co Ltd | Air-conditioning equipment subjected to antibacterial treatment |
WO2005026276A1 (en) * | 2003-09-11 | 2005-03-24 | Kabushiki Kaisha Zac | Coating material |
JPWO2005026276A1 (en) * | 2003-09-11 | 2007-11-08 | 株式会社ザック | Coating material |
JP2005254085A (en) * | 2004-03-10 | 2005-09-22 | Daicel Chem Ind Ltd | Surface-modified titanium oxide photocatalyst and method of oxidizing organic compound using it |
WO2008132807A1 (en) * | 2007-04-20 | 2008-11-06 | Panasonic Corporation | Air cleaner, and air conditioner or refrigerator using the air cleaner |
JP2009150585A (en) * | 2007-12-19 | 2009-07-09 | Sumitomo Light Metal Ind Ltd | Fin material for heat exchanger and its manufacturing method |
JP2012522965A (en) * | 2009-04-02 | 2012-09-27 | ヘンケル・アクチェンゲゼルシャフト・ウント・コムパニー・コマンディットゲゼルシャフト・アウフ・アクチェン | Automotive heat exchanger parts coated with ceramic |
JP2019116991A (en) * | 2017-12-27 | 2019-07-18 | 株式会社中部テクノ | Sterilizer of refrigeration mechanism |
KR20190128946A (en) * | 2018-05-09 | 2019-11-19 | 엘지전자 주식회사 | Coating layer |
KR102123353B1 (en) * | 2018-05-09 | 2020-06-16 | 엘지전자 주식회사 | Coating layer |
KR20210115583A (en) * | 2020-03-13 | 2021-09-27 | 오충록 | Photocatalytic Paint Composition for Ventilator and Filter Box and Manufacturing Method of thereof |
KR102389529B1 (en) | 2020-03-13 | 2022-04-21 | 오충록 | Photocatalytic Paint Composition for Ventilator and Filter Box and Manufacturing Method of thereof |
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