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JP2000325452A - Energy saving type air purifier - Google Patents

Energy saving type air purifier

Info

Publication number
JP2000325452A
JP2000325452A JP11143026A JP14302699A JP2000325452A JP 2000325452 A JP2000325452 A JP 2000325452A JP 11143026 A JP11143026 A JP 11143026A JP 14302699 A JP14302699 A JP 14302699A JP 2000325452 A JP2000325452 A JP 2000325452A
Authority
JP
Japan
Prior art keywords
catalyst
light source
air
air purification
purification device
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
JP11143026A
Other languages
Japanese (ja)
Inventor
Kiyoshi Inoue
潔 井上
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.)
Toyo Element Industry Co Ltd
Original Assignee
Toyo Element Industry Co Ltd
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 Toyo Element Industry Co Ltd filed Critical Toyo Element Industry Co Ltd
Priority to JP11143026A priority Critical patent/JP2000325452A/en
Priority to PCT/JP2000/008340 priority patent/WO2002043839A1/en
Priority claimed from PCT/JP2000/008340 external-priority patent/WO2002043839A1/en
Publication of JP2000325452A publication Critical patent/JP2000325452A/en
Pending legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L9/00Disinfection, sterilisation or deodorisation of air
    • A61L9/16Disinfection, sterilisation or deodorisation of air using physical phenomena
    • A61L9/18Radiation
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/34Chemical or biological purification of waste gases
    • B01D53/74General processes for purification of waste gases; Apparatus or devices specially adapted therefor
    • B01D53/86Catalytic processes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2255/00Catalysts
    • B01D2255/80Type of catalytic reaction
    • B01D2255/802Photocatalytic

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  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Environmental & Geological Engineering (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biomedical Technology (AREA)
  • Epidemiology (AREA)
  • Analytical Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Apparatus For Disinfection Or Sterilisation (AREA)
  • Disinfection, Sterilisation Or Deodorisation Of Air (AREA)

Abstract

PROBLEM TO BE SOLVED: To decompose harmful substances in air in a working area, and improve the environment of a living space by an inexpensive device by providing a catalyst the major component of which is titanium oxide, and which is activat ed by a noble metal, or the like, a low-powdered light source, and a power source of a small capacity to make the light source emit light. SOLUTION: This device decomposes and detoxifies harmful substances in air using a catalyst the major component of which is titanium oxide, and which is activated by a noble metal by optically activating it, and the air purifier is constituted by providing a low-powered light source to optically activate the catalyst, and a power source to make the light source emit light. For example, a cylindrical catalyst case both ends of which are open is manufactured from an aluminum pipe or a square pipe the wall surface of which is a mesh- form, and an LED is attached on the internal surface. Then, the purifier is stood at the corner in a room, and by the draft action together with the excitation of the catalyst, contaminated air in the room is convection-circulated through the inside of the case. Then, when the outside is bright, the purifying action is displayed on the outside.

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、主として居室や自
動車などの内部の空気または市街地などの空気を浄化す
る装置、特に酸化チタンを主体とし貴金属により賦活し
て成る触媒を光活性化して用い、空気中の有害物を分解
無害化処理する装置に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention mainly relates to a device for purifying air inside a living room or an automobile or the like in an urban area or the like, in particular, a photo-activated catalyst mainly composed of titanium oxide and activated by a noble metal. The present invention relates to an apparatus for decomposing and detoxifying harmful substances in air.

【0002】[0002]

【従来の技術】一般に交通の激しい市街地の交差点など
の外気や、道路近くの住宅地の空気は、多くの有機およ
び無機の有害物質によって汚染されている。それらの主
なものは例えば、 オゾンO3:300ppb〜500ppb 一酸化炭素CO:5,000ppb〜20ppm オレフイン類Cn2n(n=2〜20):400ppb〜3000ppb 窒素酸化物NOx:500ppb〜10ppm などであり、更に、20ppb〜50ppbのオーダーで、 アルデヒド R−CHO エーテル CH2−O−CH2 ブチレン C48 ケトン RCOR メタン CH4 メチルアルコール CH3OH エチレン −CH2− などが検出されている。
2. Description of the Related Art In general, the outside air at intersections of busy city areas and the air in residential areas near roads are contaminated with many organic and inorganic harmful substances. Their main thing for example, ozone O 3: 300ppb~500ppb carbon monoxide CO: 5,000ppb~20ppm olefins such C n H 2n (n = 2~20 ): 400ppb~3000ppb nitrogen oxides NOx: 500ppb~10ppm etc. , still, on the order of 20Ppb~50ppb, aldehyde R-CHO ether CH 2 -O-CH 2 butylene C 4 H 8 ketones RCOR methane CH 4 methyl alcohol CH 3 OH ethylene -CH 2 - and the like are detected .

【0003】これらの物質は健康上有害であり、各種の
アレルギー症状や、喘息、肺ガンなどを引き起こすの
で、これらを無害化する必要があるが、従来供給されて
いる民生用の空気浄化装置は、単に空気中の浮遊塵を捕
捉するもののみであり、これらの有害ガスを分解し、除
害できるものは、大電力量を必要とするものとか、太陽
光線を利用する装置などはされているが、それ以外の低
エネルギーで処理できるものは提案されていない。
[0003] These substances are harmful to health and cause various allergic symptoms, asthma, lung cancer and the like. Therefore, it is necessary to detoxify them. It only captures airborne dust in the air, and those that can decompose and remove these harmful gases include those that require large amounts of power and devices that use sunlight. However, no other low-energy process has been proposed.

【0004】[0004]

【発明が解決しようとする課題】本発明の目的とすると
ころは、人の居室や作業場内の空気中の有害物質を分解
し、生活空間の環境を改善するため利用できる、安価で
安全な民生用の空気浄化装置を提供することにある。
SUMMARY OF THE INVENTION It is an object of the present invention to provide an inexpensive and safe consumer that can be used to decompose harmful substances in the air in a person's room or work place and improve the environment of living space. An object of the present invention is to provide an air purification device for use in a vehicle.

【0005】上記の如き有害ガスを除去する目的で、工
業的に又は車両排ガス用として一般的に利用される触媒
としては、Au、Pa、Pt、Rn、Ru、Ti、Mn、Cu、W、Al、
Zr、Ce、Tb、Sm、Er、La、Dyなどと、これらの酸化物で
あるCuO、TiO2、WO3、Mn 23、Mn816、A123、Z
rO2、MnO2、Ce23、Tb23、Sm23、Er23、La2
3、Dy23などが知られており、これらは使用目的に合
わせて、単独で、又は組合わせて、更には必要に応じて
電磁波で活性化されて利用されている。
For the purpose of removing harmful gases as described above,
Catalysts commonly used industrially or for vehicle exhaust
As, Au, Pa, Pt, Rn, Ru, Ti, Mn, Cu, W, Al,
Zr, Ce, Tb, Sm, Er, La, Dy, etc. and these oxides
Some CuO, TiOTwo, WOThree, Mn TwoOThree, Mn8O16, A1TwoOThree, Z
rOTwo, MnOTwo, CeTwoOThree, TbTwoOThree, SmTwoOThree, ErTwoOThree, LaTwoO
Three, DyTwoOThreeAre known, and these are suitable for the purpose of use.
Together, alone or in combination, and as needed
It is used by being activated by electromagnetic waves.

【0006】特に有用な従来技術としては、TiO2の光
触媒が1972年に、貴金属賦活光触媒が1979年に発表され
ており、これらの応用技術についても、固体炭素類との
共用は1980年、炭水化物の分解は1980年、タンパク質、
脂肪高分子類の分解は1981年にそれぞれ発表されてい
る。特に、1〜10nmサイズの範囲の金属粒子による賦活
や、TiO2の様々な製造方法も公知である。その他Agや
希土類との組み合わせ、更にWO3系、Fe23系、CdS
系、MoS系等多くの組み合わせも発表されている。これ
らはいずれも1980年代に公知となった技術である。
As particularly useful prior arts, a TiO 2 photocatalyst was announced in 1972 and a noble metal activated photocatalyst was announced in 1979. These applied technologies were also shared with solid carbon in 1980, and carbohydrates were used. Decomposition of proteins in 1980
The decomposition of fatty polymers was published in 1981, respectively. In particular, activation by metal particles having a size in the range of 1 to 10 nm and various methods for producing TiO 2 are also known. Combination with other Ag and rare earth, further WO 3 system, Fe 2 O 3 system, CdS
Many combinations, such as a system and a MoS system, have also been announced. These are all technologies that became known in the 1980s.

【0007】[0007]

【課題を解決するための手段】而して、本発明に係る省
エネルギー型空気浄化装置は、酸化チタンを主体とし貴
金属などにより賦活して成る触媒と、その触媒を光活性
化するための低電力光源と、その光源を発光させるため
の小容量の電源とを具備する。触媒の面積には特に限定
はないが、通常は500cm2以上、10000cm2以下、望まし
くは1000cm2以上、5000cm2以下とする。又、光源の駆
動電力は触媒1cm2当たり10μW以上、15W以下、望ま
しくは触媒1cm2当たり10μW以上、100μW以下とす
る。触媒の面積が1000cm2以下であると、浄化能力が過
小となり過ぎるが、10000cm2以上とすると通常は必要
な強度を得るために要するシートの厚さが過大となるか
らである。尚、大容積の空気を浄化しようとするとき
は、大容量のもの1基よりも、上記のサイズのものを複
数用いることが望ましい。それは装置を大型とすると、
触媒面積に比して装置の内容量の増加が大きくなるた
め、相対的に触媒の接触効率が低下するからである。
又、顆粒状の触媒を用いる場合にも、上記以上に大型と
すると空気抵抗が増大するので、上記の限度に止めるこ
とが望ましい。又、光源の駆動電力を触媒1cm2当たり
10μW以下とすると処理能力が低下し過ぎ不適切となる
が、これを15mW以上としても、有害物濃度がさほど低
下せず、所要電力が浪費されるようになる。又、光源と
しては、LED、LSD、LDなどの半導体発光素子を用いるこ
とが推奨される。その理由は、光源をオンオフして使用
すると、他の光源では寿命が短くなるためである。半導
体光源はこのような使用条件で使用しても寿命が極端に
長く、また、波長が適切である上、効率が高く、高周波
の発光制御が容易であるためである。
SUMMARY OF THE INVENTION An energy-saving air purifying apparatus according to the present invention comprises a catalyst mainly composed of titanium oxide and activated by a noble metal or the like, and a low electric power for photoactivating the catalyst. It has a light source and a small-capacity power supply for causing the light source to emit light. Although there is no particular limitation on the area of the catalyst, is usually 500 cm 2 or more, 10000 cm 2 or less, preferably 1000 cm 2 or more, and 5000 cm 2 or less. The driving power of the light source catalyst 1 cm 2 per 10μW above, 15W or less, preferably catalyst 1 cm 2 per 10μW or more and less 100 .mu.W. If the area of the catalyst is 1000 cm 2 or less, the purifying ability is too small, but if it is 10,000 cm 2 or more, the thickness of the sheet required to obtain the required strength is usually too large. When purifying a large volume of air, it is preferable to use a plurality of the above sizes rather than one large volume. That is, if the device is large,
This is because the increase in the internal capacity of the device is larger than the catalyst area, and the contact efficiency of the catalyst is relatively reduced.
Also, when a granular catalyst is used, if the size is larger than the above, the air resistance increases, so it is desirable to keep the above-mentioned limit. Further, the catalyst 1 cm 2 per the driving power of the light source
If the power is set to 10 μW or less, the processing capacity is excessively reduced, which is inappropriate. However, if the power is set to 15 mW or more, the harmful substance concentration does not decrease so much, and the required power is wasted. It is recommended to use a semiconductor light emitting element such as an LED, an LSD, and an LD as a light source. The reason is that when the light source is turned on and off, the life of other light sources is shortened. This is because the semiconductor light source has an extremely long life even when used under such usage conditions, has an appropriate wavelength, is highly efficient, and easily controls high-frequency light emission.

【0008】[0008]

【発明の実施の形態】以下、使用する触媒に就いて述べ
る。例えばTiO2などの光触媒は、半導体のバンドギャ
ップの間に酸化分解される分子の酸化電位と還元電位が
存在するように電磁波を照射することにより、分解反応
が起こるものである。これは触媒の価電子帯にある原子
の電子が励起されて伝導帯に遷移し、価電子帯の部分に
はホールが残る。そして電子、ホールの対が触媒に生成
され、この電子とホールが半導体TiO2中を移動して、
電子は触媒表面に(O2 )(O2 )となって存在し、
オキサイドイオンとなり、同時に水酸ラジカル(O
)となり、還元作用と強酸化物として働き、有機物
と直接反応して有機物のC−C、C−H、C−Cl、H
−Cl等々と反応し、有機物の分解反応を起こす。一連
の作用はこのようであるが、ここで注意を要すること
は、 1.TiO2触媒の格子面欠陥の問題 2.TiO2触媒の多くの格子点欠陥の問題 3.TiO2触媒の結晶サイズの不揃いの問題 4.電子とホールの再結合の問題 についてである。
BEST MODE FOR CARRYING OUT THE INVENTION The catalyst used will be described below. For example, a photocatalyst such as TiO 2 causes a decomposition reaction by irradiating an electromagnetic wave so that an oxidation potential and a reduction potential of molecules oxidized and decomposed exist between the band gaps of a semiconductor. This is because the electrons of atoms in the valence band of the catalyst are excited and transit to the conduction band, leaving holes in the valence band. Then, a pair of an electron and a hole is generated in the catalyst, and the electron and the hole move in the semiconductor TiO 2 ,
Electrons are present as (O 2 ) (O 2 ) on the catalyst surface,
Oxide ion and hydroxyl radical (O
H + ), which acts as a reducing agent and a strong oxide, reacts directly with the organic matter, and reacts with the organic matter CC, CH, C-Cl, H
Reacts with -Cl and the like, causing decomposition reaction of organic substances. The series of actions is like this, but what should be noted here is: 1. Problem of lattice plane defect of TiO 2 catalyst 2. Problems of many lattice point defects of TiO 2 catalyst. 3. Problem of uneven crystal size of TiO 2 catalyst It is about the problem of recombination of electrons and holes.

【0009】ここで電子とホールが再結合すれば、全く
分解作用は起きないことになり、極めて効率が悪い触媒
となる。一つの触媒粒子の中で酸化還元の両反応が同時
に起こることが要求される。これらは一見矛盾している
ように見えるが、上記1〜3の問題は粒度0.1〜10nm程
度の微細な触媒TiO2を得ることにより解決でき、欠陥
を防ぐことができる。そして、これは完全結晶化のサイ
ズを形成させることで可能となる。例えば、加水分解で
析出する場合も、分解速度を精密に制御することによ
り、完全結晶化させることができる。
Here, if the electrons and holes recombine, no decomposing action occurs, and the catalyst becomes extremely inefficient. It is required that both oxidation-reduction reactions occur simultaneously in one catalyst particle. Although these seem at first glance to be contradictory, the above-mentioned problems 1 to 3 can be solved by obtaining a fine catalyst TiO 2 having a particle size of about 0.1 to 10 nm, and defects can be prevented. This is made possible by forming a size of perfect crystallization. For example, even in the case of precipitation by hydrolysis, complete crystallization can be achieved by precisely controlling the decomposition rate.

【0010】先ず始めにTiの塩化物イオンを持った多核
錯イオン液を出発原料として、0.025mol/リットルのTi
4を70℃で24時間加水分解処理し、pH6.5で尿素を添加
し、重縮合してコロイド核を形成する。粒形状は立方粒
子のアナターゼで、且つ粒形は平均10nm(電子顕微鏡像
による)となり、粒子間で強い相互作用を起こすが、塩
素を含んだ一次粒子の凝集が主体となって、粒の表面の
エネルギーを小さくしようとする力と界面張力とバラン
スした状態で粒子が形成される。
First, a polynuclear complex ion solution having Ti chloride ions is used as a starting material to obtain 0.025 mol / liter of Ti.
C 4 is hydrolyzed at 70 ° C. for 24 hours, urea is added at pH 6.5 and polycondensed to form a colloid nucleus. The particle shape is cubic anatase, and the average particle size is 10 nm (according to the electron microscope image), causing strong interaction between the particles, but the primary particles containing chlorine are mainly agglomerated. The particles are formed in a state where the force for reducing the energy of the particles and the interfacial tension are balanced.

【0011】従って、立方粒アナターゼで塩化チタンの
濃度を低く生成温度を高くした最終濃液のpHは1〜2と
する必要がある。このような条件で単核ヒドロキソ錯体
Ti−O−Tiを形成し、水洗し、乾燥させて粉砕し、微Ti
2粒子を得る。K2PtC6をメタノール水溶液にTiO2
Ptの比が重量比で1:1となるようにして懸濁し、波長
276nmの光を照射しながら、スターラーとして100kHz、6
0Wの超音波(0.1W/cm2)を照射し、強力に攪拌しな
がら処理して、酸化チタン粒子の表面にPtを析出させ
た。
Therefore, it is necessary that the pH of the final concentrated liquid obtained by lowering the concentration of titanium chloride in cubic grain anatase and raising the production temperature be 1-2. Under these conditions, mononuclear hydroxo complex
Form Ti-O-Ti, wash with water, dry and pulverize, fine Ti
Get the O 2 particles. K 2 PtC 6 with TiO 2 in methanol aqueous solution
Suspend so that the ratio of Pt is 1: 1 by weight, and
While irradiating 276nm light, 100kHz, 6 as stirrer
Irradiation with ultrasonic waves of 0 W (0.1 W / cm 2 ) was performed with strong stirring to precipitate Pt on the surface of the titanium oxide particles.

【0012】結果として、粒度10nmのTiO2粒子の表面
に、Ptが析出してTiO2Pt触媒となった。PtのサイズはT
iO2の約1/10程度の1nmオーダーとなり、Pt粒子はTi
2粒子表面に10個程度接着させることができた。この
触媒粒子を再び水と練り合わせて口径1mmのノズルから
押し出し、長さ1mmに切断してピレット化し、乾燥させ
てから300℃で3時間焼結して300〜400m2/g程度の表
面積を有する顆粒状酸化チタン触媒を得ることができ
た。なお、上記では被処理体の流通をよくするために顆
粒状としたが、勿論、膜状、板状、燐片状などとするこ
とができる。また、TiO2とSiO2の混晶を用いたり、希
土類の光励起効果を利用することも自由である。
As a result, Pt was deposited on the surface of the TiO 2 particles having a particle size of 10 nm to form a TiO 2 Pt catalyst. Pt size is T
The order of 1 nm is about 1/10 of that of SiO 2 , and Pt particles are Ti
About 10 particles could be adhered to the O 2 particle surface. The catalyst particles are again kneaded with water, extruded from a nozzle having a diameter of 1 mm, cut into a length of 1 mm, formed into a pyret, dried, and sintered at 300 ° C. for 3 hours to have a surface area of about 300 to 400 m 2 / g. A granular titanium oxide catalyst was obtained. Note that, in the above description, the object to be processed is granulated in order to improve the flow of the object, but it is needless to say that the object can be formed into a film shape, a plate shape, a scaly shape, or the like. It is also free to use a mixed crystal of TiO 2 and SiO 2 or to use the photoexcitation effect of rare earth.

【0013】最後に結晶中で電子とホールの結合の問題
は触媒として極めて重要な性能となる。勿論、反応の深
さによりその保持時間は変化する。一応この点を考慮す
れば、触媒表面が電磁波に曝されるとき、表面で起こる
反応物が内部より補給されないとし、電子とホールの放
出率をQとすれば、
Finally, the problem of electron-hole bonding in the crystal becomes a very important performance as a catalyst. Of course, the retention time varies depending on the depth of the reaction. Considering this point, if the catalyst surface is exposed to electromagnetic waves, reactants generated on the surface are not replenished from the inside, and if the emission rate of electrons and holes is Q,

【0014】[0014]

【数1】 (Equation 1)

【0015】ここでτを一定とすれば、If τ is fixed here,

【数2】 となり、電子、ホールの放出率は時定数で低下すること
を示している。
(Equation 2) This shows that the electron and hole emission rates decrease with a time constant.

【0016】実際的には、固体表面が電磁波に曝されて
いる空間は、電子、ホールの放出層が多層である場合は
異なってくる。電子ホールの放出は触媒の活性化エネル
ギーが放出量によって変わってくるので、
In practice, the space where the solid surface is exposed to the electromagnetic wave differs when the electron and hole emission layers are multilayered. Since the activation energy of the catalyst changes depending on the amount of emission,

【数3】 となる。(Equation 3) Becomes

【0017】従って、分子の振動を考慮して考察すれ
ば、結晶の生成状態によって大きく異なるが、平均的に
言えば、電子ホールの表面に滞在する時間を10−2〜10
−3とすれば、
Therefore, when considering the vibration of molecules, it greatly varies depending on the state of crystal formation. On average, however, the time spent on the surface of the electron hole is 10 −2 to 10 −10.
-3 ,

【数4】 (Equation 4)

【0018】従って、温度が20℃から100℃に上昇すれ
ば、電子及びホールの滞在時間は、10−1秒から10−3
10−4秒程度となると考えられるので、光励起の繰り返
し周期を温度に対応して電子、ホールの滞在時間に合わ
せて変化させることが推奨される。
Therefore, if the temperature rises from 20 ° C. to 100 ° C., the residence time of the electrons and holes will be from 10 −1 second to 10 −3 to 10 −3 .
Since it is considered to be about 10 −4 seconds, it is recommended that the repetition period of photoexcitation be changed according to the temperature and the residence time of electrons and holes.

【0019】電磁波照射をパルス的にした理由は、より
低電力で動作させるためである。望ましいパルス照射の
繰返し周波数は温度Tに左右されるので、効率的には温
度の関数として制御することが望ましい。
The reason why the electromagnetic wave irradiation is pulsed is to operate with lower power. Since the desired repetition frequency of pulse irradiation depends on the temperature T, it is desirable that the pulse irradiation be controlled efficiently as a function of the temperature.

【0020】また、電磁波照射の繰返し周波数の切り替
え制御にはLED、SLD、LDなどの半導体発光素子が有利で
あり、とりわけ400〜430nm程度の波長を持ったLEDが有
効である。電磁波の出力効率は、高輝度蛍光灯で91cd/
Wであるのに対し、LEDは300cd/Wと約3倍に向上す
る。更にデユーティファクタ約10%、即ちオンオフ比
1:9のパルスにして、常に電子とホールが存在してい
るようにするとき、LEDは約30倍の3000cd/Wとなり、
効率が大幅に向上する。その上、パルス照射によれば、
更に電磁波密度を高めることもできる。
Semiconductor light emitting devices such as LEDs, SLDs, and LDs are advantageous for switching control of the repetition frequency of electromagnetic wave irradiation, and LEDs having a wavelength of about 400 to 430 nm are particularly effective. The output efficiency of electromagnetic waves is 91 cd /
LED is 300 cd / W, which is about 3 times higher than W. Further, when a pulse with a duty factor of about 10%, that is, an on / off ratio of 1: 9, so that electrons and holes are always present, the LED becomes 3000 cd / W, which is about 30 times,
Efficiency is greatly improved. Moreover, according to pulsed irradiation,
Further, the electromagnetic wave density can be increased.

【0021】このように本発明によるときは、従来技術
に比べて30倍以上の効率が得られることとなる。また、
脱臭について言えば、臭気の強度をI、臭い物質の濃度
をC 0とすれば、
Thus, according to the present invention, the prior art
30 times or more of the efficiency can be obtained. Also,
Speaking of deodorization, odor intensity is I, concentration of odorous substance
To C 0given that,

【数5】 となるので、従って、脱臭には対数的に触媒作用を働か
せることが必要となる。
(Equation 5) Therefore, deodorization requires a logarithmic catalysis.

【0022】[0022]

【実施例】〔実施例1〕壁面が網状となっているアルミ
ニウム管もしくは角型管により両端の開いた筒状の触媒
ケースを製造し、内面にLEDを取り付け、室内の隅の部
分に立て掛けて、触媒の励起と共に、そのドラフト作用
により室内の汚染空気がケース内部を通って対流循環す
るようにする。又、外部が明るいときは、外側で浄化作
用が営まれる。
[Example 1] [Example 1] A tubular catalyst case having both ends opened by an aluminum tube or a square tube having a net-like wall was manufactured, LEDs were mounted on the inner surface, and the LED was mounted on a corner in the room. When the catalyst is excited, the draft action causes contaminated air in the room to convectively circulate through the interior of the case. When the outside is bright, the purifying action is performed on the outside.

【0023】このため、ケースの上端の開口は天井より
約30cm位低い位置とし、下端は床面より約50cm位高い位
置に吸入口が来るように配置する。また場合によって
は、空気を循環させるため0.05W程度のバイモルフ型フ
ァンをケース内部に挿入する場合もある。
For this reason, the upper opening of the case is arranged at a position lower than the ceiling by about 30 cm, and the lower end is arranged so that the suction port comes at a position higher by about 50 cm than the floor surface. In some cases, a bimorph fan of about 0.05 W is inserted into the case to circulate air.

【0024】内径10cm、長さ1.5mの網状壁から成る円
筒型ケースの内面にTiO2PtEr触媒を3000cm2に対して15
gの割合で塗着して、その内部に波長430nm、3cdのLED
を8個配置し、パルス状に発光させるようにした。床面
10m×5m天井高さ2.3mの部屋に垂直に設置し、オンタイ
ムを0.8msec、オフタイムを10msecとし、3.1V、ピー
ク値で42mAの電流を流してパルス状に点灯した。ケー
ス内に3.2V、0.03Wのファンを挿入し、容量12.6AH
のリチウム2次電池で駆動して0.5m3/minの室内の空
気をケース内に流し、循環させた。
TiO 2 PtEr catalyst was applied to the inner surface of a cylindrical case having a mesh wall having an inner diameter of 10 cm and a length of 1.5 m with respect to 3000 cm 2 .
g at the rate of 430nm, 3cd LED inside
Are arranged to emit light in a pulsed manner. Floor
It was installed vertically in a room with a 10m x 5m ceiling height of 2.3m, the on-time was set to 0.8msec, the off-time was set to 10msec, and a current of 3.1V, 42mA at a peak value was passed, and the lamp was turned on in a pulse shape. Insert a 3.2V, 0.03W fan into the case, with a capacity of 12.6AH
, And room air of 0.5 m 3 / min was flowed into the case and circulated.

【0025】特に注目して測定したのは、NOxで、こ
れはの反応を起こして分解される。
Of particular interest was measured NOx, which is decomposed by its reaction.

【化1】 Embedded image

【0026】測定の結果、11ppmであったケース入り口
のNOx濃度が、出口では7ppmに低下し、約41時間連続
運転後は、部屋全体の平均NOx濃度が1.1ppmとなっ
た。更に、他の種々なオレフイン、O3類の除去につい
ても、最終到達濃度が当初の約10%以下となることが判
明した。室温は平均26℃で、湿度は60%であった。尚、
部屋は1日の車両等の通過台数が平均14万台の交差点に
面しており、4人の人が普通に生活し、出入りも自由に
させていた。
As a result of the measurement, the NOx concentration at the entrance of the case was reduced from 11 ppm to 7 ppm at the exit, and after continuous operation for about 41 hours, the average NOx concentration in the entire room became 1.1 ppm. Further, it was also found that the final concentration reached about 10% or less of the removal of various other olefins and O 3 . Room temperature averaged 26 ° C and humidity was 60%. still,
The room faces an intersection with an average of 140,000 vehicles passing through the city each day. Four people lived normally and were allowed to enter and exit freely.

【0027】上記のリチウム2次電池で連続10日間再充
電なしで駆動できた。補助電源として太陽電池を併用し
た場合は、1カ月連続使用できた。どちらの場合も、上
記と略同様に、当初の約1/10の濃度まで有害物を除去
できることが立証された。
The above lithium secondary battery was able to be driven without recharging for 10 consecutive days. When a solar cell was used together as an auxiliary power source, it could be used for one month continuously. In both cases, it was proved that the harmful substances could be removed up to about 1/10 of the original concentration almost in the same manner as described above.

【0028】〔実施例2〕上記の微粒状触媒を、多孔フ
ツ素樹脂に重量比で50%となるよう配合し、練り合わせ
て、圧延し、厚さ0.1mmのシートとし、このシート1000c
mを成形して外灯の部分より5cmの位置に取り付け、
夜間の外灯点灯中はその光で、昼間は太陽光で触媒を賦
活するようにしたとき、1昼夜の平均で、0.42μmol/c
m2・hの硝酸発生を検出した。外灯用の場合は、高速道
路、交通渋滞地域の都市道路、トンネル内部などで無電
源で利用できるが、太陽電池との併用が有利となる。道
路の防音壁に組み込むことも有効である。
Example 2 The above-mentioned finely divided catalyst was mixed with a porous fluororesin so as to have a weight ratio of 50%, kneaded and rolled to form a sheet having a thickness of 0.1 mm.
by molding the m 2 attached to 5cm position than the portion of the outdoor lights,
When the catalyst is activated by the light while the external light is lit at night and by sunlight during the day, the average of one day and night is 0.42 μmol / c.
The generation of m 2 · h nitric acid was detected. In the case of an outside light, it can be used without a power source on an expressway, an urban road in a traffic congestion area, inside a tunnel, and the like, but it is advantageous to use the solar cell together. It is also effective to incorporate it into the noise barrier of the road.

【0029】屋内の電灯、蛍光灯等の反射板に取り付け
るとこれらは無電源利用が可能となる。この場合も勿論
太陽電池との併用が有効である。尚、触媒の形状などは
任意に設計することができる。更にまた、導電度を測定
するメータ、自動点灯スイッチ、ブザー等を付属させ
て、反応状態を検定できるようにすればより有効に利用
できるようになる。
When mounted on a reflector such as an indoor light or a fluorescent light, these can be used without power supply. In this case, of course, the combined use with a solar cell is effective. The shape of the catalyst can be arbitrarily designed. Furthermore, if a meter for measuring the conductivity, an automatic lighting switch, a buzzer, and the like are attached so that the reaction state can be verified, it can be used more effectively.

【0030】この触媒はダイオキシン類についても分解
効果があり、ダイオキシン類は塩化物、硼化物及び酸化
物に分解できる。また、不完全燃焼によるCOガスに対
しても有効で、この場合は排気を水洗処理するような組
み合わせが有利となる。更に、防毒マスクとしても利用
でき、病院等においても殺菌作用と脱臭作用を得ること
ができる。これらは小型電池駆動でも1カ月以上連続駆
動できるので、極めて有効である。
This catalyst has a decomposing effect on dioxins, which can be decomposed into chlorides, borides and oxides. It is also effective for CO gas due to incomplete combustion. In this case, a combination in which exhaust gas is washed with water is advantageous. Further, it can be used as a gas mask, and can have a sterilizing action and a deodorizing action even in hospitals and the like. These are extremely effective because they can be driven continuously for one month or more even with a small battery drive.

【0031】[0031]

【発明の効果】本発明は、極めて低いエネルギーで有機
物等を高能率に分解することができ、屋内外の空気中の
有害物を少しずつ分解し、連続的に浄化できる装置とし
て効果が大きく、応用の範囲も広い。
Industrial Applicability The present invention is highly effective as a device capable of decomposing organic substances and the like with very low energy at a high efficiency, decomposing harmful substances in indoor and outdoor air little by little, and purifying continuously. Wide range of applications.

Claims (10)

【特許請求の範囲】[Claims] 【請求項1】 酸化チタンを主体とし貴金属などにより
賦活して成る触媒と、その触媒を光活性化するための低
電力光源と、その光源を発光させるための電源とを具備
する省エネルギー型空気浄化装置。
An energy-saving air purification system comprising a catalyst mainly composed of titanium oxide and activated by a noble metal, a low-power light source for photoactivating the catalyst, and a power supply for causing the light source to emit light. apparatus.
【請求項2】 光源の駆動電力が触媒1cm2当たり10μ
W以上、15mW以下である請求項1に記載の空気浄化装
置。
2. The driving power of the light source is 10 μm / cm 2 of the catalyst.
2. The air purification device according to claim 1, wherein the air purification device is not less than W and not more than 15 mW.
【請求項3】 光源が半導体発光素子である請求項1又
は2に記載の空気浄化装置。
3. The air purification device according to claim 1, wherein the light source is a semiconductor light emitting device.
【請求項4】 電源がパルス電源である請求項1ないし
3の何れか一に記載の空気浄化装置。
4. The air purifying apparatus according to claim 1, wherein the power supply is a pulse power supply.
【請求項5】 電源のパルスの繰り返し周波数が、温度
によって変化せしめられる請求項1ないし4の何れか一
に記載の空気浄化装置。
5. The air purifying apparatus according to claim 1, wherein the repetition frequency of the pulse of the power supply is changed according to the temperature.
【請求項6】 触媒が、両端が開放された筒状に形成さ
れ、光源がその簡状触媒の内部に配置され、筒状触媒が
その内外に対流を起こすように設置されて用いられる、
請求項1ないし5の何れか一に記載の空気浄化装置。
6. The catalyst is formed in a tubular shape with both ends open, a light source is disposed inside the simple catalyst, and the tubular catalyst is installed and used so as to cause convection inside and outside thereof.
An air purification device according to any one of claims 1 to 5.
【請求項7】 筒状触媒の内部に、低エネルギーファン
を設けた請求項6に記載の空気浄化装置。
7. The air purification device according to claim 6, wherein a low-energy fan is provided inside the tubular catalyst.
【請求項8】 筒状触媒の空気取り入れ口に、フィルタ
ーを設けた請求項6又は7に記載の空気浄化装置。
8. The air purification device according to claim 6, wherein a filter is provided in an air intake of the cylindrical catalyst.
【請求項9】 触媒を表裏両面より光活性化する請求項
1ないし8の何れか一に記載の空気浄化装置。
9. The air purification device according to claim 1, wherein the catalyst is photoactivated from both front and back surfaces.
【請求項10】 酸化チタンを主体とし貴金属により賦
活して成る触媒を、照明灯の反射板の表面に設けて成る
空気浄化装置。
10. An air purification device comprising a catalyst mainly composed of titanium oxide and activated by a noble metal, provided on the surface of a reflector of an illumination lamp.
JP11143026A 1999-05-24 1999-05-24 Energy saving type air purifier Pending JP2000325452A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP11143026A JP2000325452A (en) 1999-05-24 1999-05-24 Energy saving type air purifier
PCT/JP2000/008340 WO2002043839A1 (en) 1999-05-24 2000-11-27 Energy saving air cleaner

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP11143026A JP2000325452A (en) 1999-05-24 1999-05-24 Energy saving type air purifier
PCT/JP2000/008340 WO2002043839A1 (en) 1999-05-24 2000-11-27 Energy saving air cleaner

Publications (1)

Publication Number Publication Date
JP2000325452A true JP2000325452A (en) 2000-11-28

Family

ID=26344976

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JP2000325452A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002043839A1 (en) * 1999-05-24 2002-06-06 Toyo Element Industry Co., Ltd. Energy saving air cleaner

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01139139A (en) * 1987-11-26 1989-05-31 Nippon Sheet Glass Co Ltd Deodorization/sterilization equipment
JPH09940A (en) * 1995-06-19 1997-01-07 Toyoda Gosei Co Ltd Photocatalytst device and its application device
JPH09140782A (en) * 1995-11-22 1997-06-03 Sharp Corp Illuminator provided with air purifying function

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01139139A (en) * 1987-11-26 1989-05-31 Nippon Sheet Glass Co Ltd Deodorization/sterilization equipment
JPH09940A (en) * 1995-06-19 1997-01-07 Toyoda Gosei Co Ltd Photocatalytst device and its application device
JPH09140782A (en) * 1995-11-22 1997-06-03 Sharp Corp Illuminator provided with air purifying function

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002043839A1 (en) * 1999-05-24 2002-06-06 Toyo Element Industry Co., Ltd. Energy saving air cleaner

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