JPH0822393B2 - Particle charging / collecting unit device - Google Patents
Particle charging / collecting unit deviceInfo
- Publication number
- JPH0822393B2 JPH0822393B2 JP26128991A JP26128991A JPH0822393B2 JP H0822393 B2 JPH0822393 B2 JP H0822393B2 JP 26128991 A JP26128991 A JP 26128991A JP 26128991 A JP26128991 A JP 26128991A JP H0822393 B2 JPH0822393 B2 JP H0822393B2
- Authority
- JP
- Japan
- Prior art keywords
- emitting material
- photoelectron emitting
- ultraviolet
- electrode
- photoelectron
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 239000002245 particle Substances 0.000 title claims description 17
- 239000000463 material Substances 0.000 claims description 93
- 239000010419 fine particle Substances 0.000 claims description 45
- 239000011521 glass Substances 0.000 claims description 6
- 239000012780 transparent material Substances 0.000 claims 1
- 230000005684 electric field Effects 0.000 description 29
- 238000004140 cleaning Methods 0.000 description 23
- 239000000126 substance Substances 0.000 description 14
- 239000007772 electrode material Substances 0.000 description 13
- 239000010409 thin film Substances 0.000 description 12
- 229910045601 alloy Inorganic materials 0.000 description 9
- 239000000956 alloy Substances 0.000 description 9
- 238000000034 method Methods 0.000 description 9
- 239000010931 gold Substances 0.000 description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- 238000010586 diagram Methods 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 230000001954 sterilising effect Effects 0.000 description 5
- 229910052709 silver Inorganic materials 0.000 description 4
- 229910017518 Cu Zn Inorganic materials 0.000 description 3
- 229910017752 Cu-Zn Inorganic materials 0.000 description 3
- 229910017943 Cu—Zn Inorganic materials 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- 229910052790 beryllium Inorganic materials 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- TVZPLCNGKSPOJA-UHFFFAOYSA-N copper zinc Chemical compound [Cu].[Zn] TVZPLCNGKSPOJA-UHFFFAOYSA-N 0.000 description 3
- 239000010408 film Substances 0.000 description 3
- 230000010354 integration Effects 0.000 description 3
- 230000001678 irradiating effect Effects 0.000 description 3
- 229910052749 magnesium Inorganic materials 0.000 description 3
- 239000004065 semiconductor Substances 0.000 description 3
- 229910000906 Bronze Inorganic materials 0.000 description 2
- 229910052788 barium Inorganic materials 0.000 description 2
- 239000010974 bronze Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000004659 sterilization and disinfection Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- 229910000497 Amalgam Inorganic materials 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- 229910052684 Cerium Inorganic materials 0.000 description 1
- 229910052688 Gadolinium Inorganic materials 0.000 description 1
- 229910021193 La 2 O 3 Inorganic materials 0.000 description 1
- 229910017493 Nd 2 O 3 Inorganic materials 0.000 description 1
- 229910052779 Neodymium Inorganic materials 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 229910052777 Praseodymium Inorganic materials 0.000 description 1
- -1 ThO 2 Inorganic materials 0.000 description 1
- 229910052776 Thorium Inorganic materials 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- MXCPYJZDGPQDRA-UHFFFAOYSA-N dialuminum;2-acetyloxybenzoic acid;oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3].CC(=O)OC1=CC=CC=C1C(O)=O MXCPYJZDGPQDRA-UHFFFAOYSA-N 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 230000003631 expected effect Effects 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229910052746 lanthanum Inorganic materials 0.000 description 1
- 229910052745 lead Inorganic materials 0.000 description 1
- 238000010907 mechanical stirring Methods 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 150000001247 metal acetylides Chemical class 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000013618 particulate matter Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Landscapes
- Electrostatic Separation (AREA)
Description
【0001】[0001]
【産業上の利用分野】本発明は、空間清浄化のための清
浄装置と方法に係り、特に空間中に存在する微粒子を光
電子を用いて荷電・捕集する荷電・捕集ユニット装置と
それを用いた荷電・捕集方法に関する。本発明の荷電・
捕集ユニット装置と、それを用いた方法は、微粒子を荷
電・捕集(除去)して、清浄化気体あるいは清浄化空間
を得る分野に利用できる。例えば、家庭、事務所、病
院、あるいは半導体工業、薬品工業、食品工業、農林産
業、医薬、精密機械工業等各種産業におけるクリーンル
ーム、無菌室等における空間や、安全キャビネット、ク
リーンボックス、貴重品の保管庫、ウェハ保管庫、貴重
品の密閉搬送空間等におけるクリーンな密閉空間(各種
気体の存在下あるいは真空中)、各種CVD装置、各種
成膜装置関連における空間の清浄化等である。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a cleaning device and method for cleaning a space, and more particularly to a charging / collecting unit device for charging / collecting fine particles existing in a space by using photoelectrons. The charge / collection method used. Charge of the present invention
The collection unit device and the method using the same can be used in the field of charging and collecting (removing) fine particles to obtain a clean gas or a clean space. For example, clean rooms in various industries such as homes, offices, hospitals, semiconductor industry, pharmaceutical industry, food industry, agriculture and forestry industry, pharmaceuticals, precision machinery industry, aseptic rooms, safety cabinets, clean boxes, storage of valuables. It is a clean closed space (in the presence of various gases or in a vacuum) in a storage, a wafer storage, a sealed transfer space for valuables, etc., cleaning of various CVD devices, and spaces related to various film forming devices.
【0002】[0002]
【従来の技術】光電子放出材に、紫外線を照射すること
により発生する光電子による微粒子の荷電・捕集につい
ては、先に本発明者の多数の提案がある。本発明者が空
間の浄化関係において提案したものの内、本発明と特に
関連性を有するものには次のものがある。(1)特公告
平3−5859号公報(Us patent 4,750,917
号)、(2)特開昭63−77557号公報、(3)特
開昭63−100955号公報、(4)特開平2−10
034号公報、(5)特願平2−295422号、
(6)特願平3−22685号。さらに、荷電条件関係
において提案したものには、(1)特開平2−8639
号公報、(2)特願平1−120563号。さらに、光
電子放出材関係において提案したものに、(1)特開平
2−8638号公報、(2)特願平1−155857
号、(3)特願平1−153335号、(4)特願平2
−278123号、(5)特願平2−295423号が
ある。2. Description of the Related Art Many proposals have been made by the present inventor for charging and collecting fine particles by photoelectrons generated by irradiating a photoelectron emitting material with ultraviolet rays. Among the things that the present inventor has proposed in relation to space purification, the following are particularly relevant to the present invention. (1) Us patent 4,750,917
No.), (2) JP-A-63-77557, (3) JP-A-63-100955, (4) JP-A-2-10.
No. 034, (5) Japanese Patent Application No. 2-295422.
(6) Japanese Patent Application No. 3-22685. Further, regarding the charging conditions, there are (1) JP-A-2-8639.
(2) Japanese Patent Application No. 1-120563. In addition, the proposals relating to photoelectron emitting materials include (1) Japanese Patent Application Laid-Open No. 2-8638 and (2) Japanese Patent Application No. 1-155857.
No. 1, (3) Japanese Patent Application No. 1-153335, (4) Japanese Patent Application No. 2
No. 278123 and (5) Japanese Patent Application No. 2-295423.
【0003】[0003]
【発明が解決しようとする課題】上記従来の光電子によ
る微粒子の荷電・捕集は、紫外線源、光電子放出材、電
極を個別に設置して用いていた。すなわち、紫外線源、
光電子放出材、電極が離れて設置されていたので、利用
分野によっては改善の余地があった。また、清浄化装置
の設計において、紫外線源、光電子放出材、電極が一体
化していれば、取扱いが容易となり、清浄化がコンパク
トにできるなど、実用上有利となる。In the above-mentioned conventional charging / collecting of fine particles by photoelectrons, an ultraviolet source, a photoelectron emitting material, and an electrode are individually installed and used. That is, an ultraviolet source,
Since the photoemissive material and the electrodes were installed separately, there was room for improvement depending on the field of application. Further, in the design of the cleaning device, if the ultraviolet source, the photoelectron emitting material, and the electrode are integrated, the handling becomes easy and the cleaning becomes compact, which is practically advantageous.
【0004】上記課題を以下に例をあげて説明する。図
4は、半導体産業におけるウェハ保管庫における微粒子
除去の作用を示す構成図である。ウェハ保管庫1は、紫
外線ランプ2、光電子放出材3、電場設定用電極材4、
紫外線ランプ2からの紫外線の反射面5から構成されて
いる。ウェハ保管庫1中の微粒子6は、紫外線ランプ2
の照射を受けた光電子放出材3から放出される光電子7
により荷電され、荷電微粒子8となる。該荷電微粒子8
は、電場設定用電極材4にて捕集される。ここで、ウェ
ハ保管庫1は密閉空間であるので、、電場設定用電極材
4は荷電微粒子の捕集材の役目をしている。9はウェハ
キャリャー、10はウェハを示す。ここでの光電子放出
材は本発明者がすでに提案した(特願平2−29542
3号)紫外線透過性物質の表面に光電子を放出する物質
を薄膜状に付加したものであり、図4ではガラス材の表
面に50ÅAuを付加したものである。The above problem will be described below with reference to examples. FIG. 4 is a configuration diagram showing an operation of removing fine particles in a wafer storage in the semiconductor industry. The wafer storage 1 includes an ultraviolet lamp 2, a photoelectron emitting material 3, an electric field setting electrode material 4,
It is composed of a reflecting surface 5 for the ultraviolet rays from the ultraviolet lamp 2. The particles 6 in the wafer storage 1 are UV lamps 2.
Photoelectrons 7 emitted from the photoelectron emission material 3 irradiated with
And become charged fine particles 8. The charged fine particles 8
Are collected by the electric field setting electrode material 4. Here, since the wafer storage 1 is a closed space, the electric field setting electrode material 4 serves as a collector for the charged fine particles. Reference numeral 9 indicates a wafer carrier, and 10 indicates a wafer. The photoelectron emitting material here has already been proposed by the present inventor (Japanese Patent Application No. 29542/1990).
No. 3) A substance that emits photoelectrons is added to the surface of an ultraviolet-transparent substance in the form of a thin film. In FIG. 4, 50ÅAu is added to the surface of a glass material.
【0005】この様な場合、紫外線ランプ、光電子放出
材、電極材が個別に設置されるため、 紫外線ランプ
2は、ウェハ保管庫1の外側に設置されるので、放出紫
外線が有効に光電子放出材3に照射されない(例、光電
子放出材3に対し、反射面方向の紫外線はロスが大き
い)。また、 電場(電界)は光電子放出材3と電極
材4の間に設定されるため、(a)ウェハが電場中に設
置されるので、ウェハの状態によっては(例、表面が活
性化されている場合)電場の作用に影響を受ける場合が
ある。また、(b)光電子放出材3と電極材4の距離が
長いので、電場設定のための印加電圧が高くなる課題が
あり、改善の余地があった。そこで、本発明は、上記課
題を解決し、微粒子の荷電・捕集を効果的に行うことの
できる微粒子の荷電・捕集ユニット装置及び該荷電・捕
集ユニットを用いる微粒子の荷電・捕集方法を提供する
ことを目的とする。In such a case, since the ultraviolet lamp, the photoelectron emitting material, and the electrode material are individually installed, the ultraviolet lamp 2 is installed outside the wafer storage 1, so that the emitted ultraviolet light is effectively emitted. 3 is not irradiated (for example, with respect to the photoelectron emitting material 3, ultraviolet rays in the direction of the reflecting surface have a large loss). In addition, since the electric field (electric field) is set between the photoelectron emitting material 3 and the electrode material 4, (a) the wafer is placed in the electric field, and depending on the state of the wafer (eg, the surface is activated, If there is) it may be affected by the action of the electric field. Further, (b) since the distance between the photoelectron emitting material 3 and the electrode material 4 is long, there is a problem that the applied voltage for setting the electric field becomes high, and there is room for improvement. Therefore, the present invention solves the above-mentioned problems, and a particle charging / collecting unit device capable of effectively charging / collecting particles and a method of charging / collecting particles using the charging / collecting unit. The purpose is to provide.
【0006】[0006]
【課題を解決するための手段】上記目的を解決するため
に、本発明では、光電子による空間中の微粒子の荷電・
捕集ユニット装置において、紫外線源と光電子放出材及
び電極からなり、該紫外線源が棒状の紫外線ランプであ
り、該ランプを筒状の光電子放出材と金網電極で囲み一
体化してユニット化したことを特徴とする微粒子の荷電
・捕集ユニット装置としたものである。また、本発明で
は、上記荷電・捕集ユニットを微粒子が存在する空間中
に設置することを特徴とした空間中の微粒子の荷電・捕
集方法としたものである。上記における一体化では、
紫外線源を光電子放出材で囲み、 更にその近傍に
(電場用)電極を設置し、 光電子放出材又は電極の
少なくともいずれか一方の形状を、清浄化空間部に存在
する微粒子が光電子放出部から放出された光電子により
荷電されるように、該光電子放出部に移動できるように
したものである。In order to solve the above-mentioned object, in the present invention, the charge / charge of fine particles in space by photoelectrons is performed.
In the collection unit device, an ultraviolet source, a photoelectron emitting material, and an electrode are used , and the ultraviolet source is a rod-shaped ultraviolet lamp.
According to another aspect of the present invention, there is provided a fine particle charging / collecting unit device in which the lamp is surrounded by a cylindrical photoelectron emitting material and a wire mesh electrode to be integrated into a unit. Further, the present invention provides a method of charging / collecting fine particles in a space, characterized in that the charging / collecting unit is installed in a space in which fine particles are present. In the above integration,
The UV source is surrounded by a photoelectron emitting material, and an electrode (for an electric field) is installed in the vicinity of the ultraviolet light source, and at least one of the shape of the photoelectron emitting material and the electrode is discharged from the photoelectron emitting portion by the fine particles present in the cleaning space. The photoelectron emitting portion can be moved to the photoelectron emitting portion so as to be charged by the generated photoelectrons.
【0007】本発明の光電子による空間中微粒子の荷電
・捕集ユニットの例を図1及び図2に示す。図1におい
て、本発明の微粒子の荷電・捕集ユニットは、紫外線源
として紫外線ランプ(棒状)11、該ランプを囲む形状
(筒状)のガラス母材12上の光電子放出材13、該光
電子放出材13を囲む形状(筒状)の金網電極14より
なる。光電子放出材13は、紫外線透過性物質である石
英ガラス12の表面に薄膜状に付加されており、紫外線
ランプ11からの紫外線照射により、光電子15を円周
方向に放射状に放出する。該光電子の放出は、後述のご
とく、電場での紫外線照射で効果的となるため、光電子
放出材13(−極)と電極14(+極)間に電場を形成
している(光電子放出部)。An example of a charge / collection unit of particles in space by photoelectrons according to the present invention is shown in FIGS. 1 and 2. In FIG. 1, the particle charging / collecting unit of the present invention comprises an ultraviolet lamp (rod) 11 as an ultraviolet source, a photoelectron emitting material 13 on a glass base material 12 in a shape surrounding the lamp (cylindrical), and the photoelectron emitting material. The wire mesh electrode 14 has a shape (cylindrical shape) surrounding the material 13. The photoelectron emission material 13 is added in a thin film form on the surface of the quartz glass 12 which is an ultraviolet ray transmitting substance, and emits photoelectrons 15 radially in the circumferential direction by irradiation of ultraviolet rays from the ultraviolet ray lamp 11. As will be described later, the emission of the photoelectrons is effective by irradiation with ultraviolet rays in an electric field, so that an electric field is formed between the photoelectron emitting material 13 (− pole) and the electrode 14 (+ pole) (photoelectron emitting portion). .
【0008】電極14は、上述のごとく電場形成のため
と同時に、荷電微粒子の捕集材としての役目をする。す
なわち、光電子放出部から放出された光電子15により
後述のごとく近傍に浮遊する微粒子は荷電され、荷電微
粒子となり、電極14に捕集され、近傍の空間は清浄化
される。図2に、別の形状の荷電・捕集ユニットを示
す。図2の荷電・捕集ユニットは、紫外線ランプ(棒
状)21、該ランプを囲む形状(筒状)の金網電極2
2、該金網電極22を囲む形状(筒状)の金網状光電子
放出材23よりなる。光電子放出材23と電極22間に
電場を形成しており、光電子放出材23へ紫外線照射す
ることにより光電子24が放出される。The electrode 14 serves not only for forming an electric field as described above, but also as a collector for charged fine particles. That is, the photoelectrons 15 emitted from the photoelectron emitting portion charge the fine particles floating in the vicinity as described later, and become charged fine particles, which are collected by the electrode 14 and the nearby space is cleaned. FIG. 2 shows another shape of the charging / collecting unit. The charging / collecting unit shown in FIG. 2 includes an ultraviolet lamp (bar-shaped) 21 and a wire mesh electrode 2 surrounding the lamp (cylindrical).
2. The wire mesh photoelectron emitting material 23 has a shape (cylindrical shape) surrounding the wire mesh electrode 22. An electric field is formed between the photoelectron emitting material 23 and the electrode 22, and photoelectrons 24 are emitted by irradiating the photoelectron emitting material 23 with ultraviolet rays.
【0009】次に、本発明の夫々の構成を詳細に説明す
る。光電子放出材は、紫外線照射により光電子を放出す
るものであれば何れでも良く、光電的な仕事関数が小さ
なもの程好ましい、効果や経済性の面から、Ba,S
r,Ca,Y,Gd,La,Ce,Nd,Th,Pr,
Be,Zr,Fe,Ni,Zn,Cu,Ag,Pt,C
d,Pb,Al,C,Mg,Au,In,Bi,Nb,
Si,Ta,Ti,U,B,Eu,Sn,P,Wのいず
れか又はこれらの化合物又は合金が好ましく、これらは
単独で又は二種以上を複合して用いられる。複合材とし
ては、アマルガムの如く物理的な複合材も用いうる。例
えば、化合物としては酸化物、ほう化物、炭化物があ
り、酸化物にはBaO,SrO,CaO,Y2 O5 ,G
d2 O3 、Nd2 O3、ThO2 、ZrO2 、Fe2 O
3 、ZnO,CuO,Ag2 O,La2 O3 ,PtO,
PbO,Al2 O3 ,MgO,In2 O3 ,BiO,N
bO,BeOなどがあり、またほう化物にはYB6 ,C
dB6 ,LaB5 ,NdB6 ,CeB6 ,EuB6 ,P
rB6 ,ZrB2 などがあり、さらに炭化物としてはU
C,ZrC,TaC,TiC,NbC,WCなどがあ
る。Next, the respective constitutions of the present invention will be explained in detail. The photoelectron emitting material may be any material as long as it emits photoelectrons upon irradiation with ultraviolet light, and a material having a smaller photoelectric work function is more preferable.
r, Ca, Y, Gd, La, Ce, Nd, Th, Pr,
Be, Zr, Fe, Ni, Zn, Cu, Ag, Pt, C
d, Pb, Al, C, Mg, Au, In, Bi, Nb,
Any one of Si, Ta, Ti, U, B, Eu, Sn, P, W or a compound or alloy thereof is preferable, and these are used alone or in combination of two or more kinds. As the composite material, a physical composite material such as amalgam can also be used. For example, compounds include oxides, borides, and carbides, and oxides include BaO, SrO, CaO, Y 2 O 5 , and G.
d 2 O 3 , Nd 2 O 3 , ThO 2 , ZrO 2 , Fe 2 O
3 , ZnO, CuO, Ag 2 O, La 2 O 3 , PtO,
PbO, Al 2 O 3 , MgO, In 2 O 3 , BiO, N
bO, BeO, etc., and boride contains YB 6 , C
dB 6 , LaB 5 , NdB 6 , CeB 6 , EuB 6 , P
rB 6 , ZrB 2 and the like, and further U as a carbide
C, ZrC, TaC, TiC, NbC, WC and the like.
【0010】また、合金としては黄銅、青銅、リン青
銅、AgとMgとの合金(Mgが2〜20wt%)、C
uとBeとの合金(Beが1〜10wt%)及びBaと
Alとの合金を用いることができ、上記AgとMgとの
合金、CuとBeとの合金及びBaとAlとの合金が好
ましい。酸化物は金属表面のみを空気中で加熱したり、
或いは薬品で酸化することによっても得ることができ
る。さらに他の方法としては使用前に加熱し、表面に酸
化層を形成して長期にわたって安定な酸化層を得ること
もできる。この例としてはMgとAgとの合金を水蒸気
中で300〜400℃の温度の条件下でその表面に酸化
膜を形成させることができ、この酸化薄膜は長期間にわ
たって安定なものである。As the alloy, brass, bronze, phosphor bronze, an alloy of Ag and Mg (Mg is 2 to 20 wt%), C
An alloy of u and Be (1 to 10 wt% of Be) and an alloy of Ba and Al can be used, and the alloy of Ag and Mg, the alloy of Cu and Be, and the alloy of Ba and Al are preferable. . Oxide heats only the metal surface in air,
Alternatively, it can be obtained by oxidizing with a chemical. As another method, it is also possible to heat before use to form an oxide layer on the surface to obtain a stable oxide layer for a long period of time. As an example of this, an alloy of Mg and Ag can form an oxide film on its surface in water vapor at a temperature of 300 to 400 ° C., and this oxide thin film is stable for a long period of time.
【0011】また、光電子を放出する物質を別の物質に
付加して使用することができる。この例として、紫外線
透過性物質に光電子を放出し得る物質を付加したものが
ある。図1の例では紫外線透過性物質(母材)としての
石英ガラス上に光電子を放出し得る物質として、Auを
薄膜状に付加したものである(特願平2−295423
号)。図2の例では、金網状のCu−ZnにAuを薄膜
状に付加したものである。光電子放出材の形状や構造は
後述のごとく、装置(ユニット)の形状、構造あるいは
希望する効果等により異なり、適宜決めることができ
る。光電子放出材からの光電子放出のための照射源は、
照射により光電子を放出するものであればいずれでも良
いが、効果、操作性の面で、紫外線が通常好ましい。Further, a substance that emits photoelectrons can be used by adding it to another substance. An example of this is an ultraviolet-transparent substance to which a substance capable of emitting photoelectrons is added. In the example of FIG. 1, Au is added in a thin film form as a substance capable of emitting photoelectrons on quartz glass as an ultraviolet ray transmissive substance (base material) (Japanese Patent Application No. 2-295423).
issue). In the example of FIG. 2, Au is added in the form of a thin film to the wire mesh Cu—Zn. The shape and structure of the photoelectron emitting material differ depending on the shape and structure of the device (unit), desired effect, and the like, as described later, and can be appropriately determined. The irradiation source for photoelectron emission from the photoelectron emitting material is
Irradiation may be any one as long as it emits photoelectrons by, but effective, in terms of operability, UV is generally preferred.
【0012】紫外線の種類は、その照射により光電子放
出材が光電子を放出しうるものであれば何れでも良く、
適用分野によっては、殺菌(滅菌)作用を併せてもつも
のが好ましい。紫外線の種類は、適用分野、作業内容、
用途、経済性などにより適宜決めることができる。例え
ば、バイオロジカル分野においては、殺菌作用、効率の
面から遠紫外線を併用するのが好ましい。該紫外線源と
しては、紫外線を発するものであれば何れも使用でき、
適用分野、装置の形状、構造、効果、経済性等により適
宜選択し用いることができる。例えば、水銀灯、水素放
電管、キセノン放電管、ライマン放電管などを適宜使用
できる。バイオロジカル分野では、殺菌(滅菌)波長2
54nmを有する紫外線を用いると、殺菌(滅菌)効果
が併用でき好ましい。Any kind of ultraviolet light may be used as long as the photoelectron emitting material can emit photoelectrons by its irradiation.
Depending on the field of application, those having a sterilizing action are also preferable. The type of UV light depends on the application field, work content,
It can be appropriately determined depending on the use, economy and the like. For example, in the biological field, it is preferable to use deep ultraviolet rays together from the viewpoint of bactericidal action and efficiency. As the ultraviolet ray source, any one can be used as long as it emits ultraviolet rays,
It can be appropriately selected and used depending on the application field, the shape of the device, the structure, the effect, the economical efficiency and the like. For example, a mercury lamp, a hydrogen discharge tube, a xenon discharge tube, a Lyman discharge tube, or the like can be used as appropriate. In the biological field, sterilization wavelength 2
It is preferable to use an ultraviolet ray having a wavelength of 54 nm because the sterilizing effect can be used together.
【0013】次に、本発明の特徴である紫外線源、光電
子放出材、電極の位置や形状について述べる。これら
は、紫外線源を囲み設置され、微粒子の荷電・捕集器
(ユニット)として一体化していることに特徴がある。
光電子放出材の位置や形状は、紫外線源から放出される
紫外線を囲むように(照射面積が広くできるように)設
置できるものであればいずれでも良い。通常、紫外線源
からの紫外線は円周方向に放射状に放出されるため、こ
の紫外線を囲むように円周方向に設置できるものであれ
ば良い。Next, the positions and shapes of the ultraviolet ray source, the photoelectron emitting material, and the electrodes, which are the features of the present invention, will be described. These are characterized in that they are installed around an ultraviolet source and integrated as a charging / collecting unit (unit) for fine particles.
The position and shape of the photoelectron emitting material may be any as long as they can be installed so as to surround the ultraviolet rays emitted from the ultraviolet ray source (to increase the irradiation area). Normally, the ultraviolet rays from the ultraviolet source are radially emitted in the circumferential direction, and thus any material that can be installed in the circumferential direction so as to surround the ultraviolet rays may be used.
【0014】次に、電極の位置や形状は、光電子放出材
との間に電場(電界)が形成できるものであれば何れも
使用できる。電極材料とその構造は、周知の荷電装置に
おいて使用されているもので良い。電極材料は導体であ
れば何れも使用でき、この例としてタングステンの金網
がある。これを光電子放出材の近傍に電場が形成できる
よう設置する。電極の位置に対する光電子放出材の位置
は、図1のように紫外線ランプの近傍側、あるいは図2
のように紫外線ランプの対向側(処理空間側)にと、適
宜の位置に光電子放出材の種類や形状、利用分野、装置
形状、規模、効果、経済性などにより決めることができ
る。Next, any position and shape of the electrode can be used as long as an electric field can be formed between the electrode and the photoelectron emitting material. The electrode material and its structure may be those used in known charging devices. Any electrode material can be used as long as it is a conductor, and an example thereof is a tungsten wire mesh . This is installed so that an electric field can be formed near the photoelectron emitting material. The position of the photoelectron emitting material relative to the position of the electrode is near the ultraviolet lamp as shown in FIG.
As described above, it can be determined depending on the type and shape of the photoelectron emitting material, the field of use, the shape of the device, the scale, the effect, the economic efficiency, etc., on the opposite side (processing space side) of the ultraviolet lamp.
【0015】光電子放出材の種類は、本発明者がすでに
提案したように板状のもの、プリーツ状のもの、金網状
のもの(特開昭61−178050号公報)、母材上に
保護膜を付加したもの(特願平1−155857号)、
薄膜の形状のもの(特願平2−278123号)、紫外
線透過性物質に付加したもの(特願平2−295423
号)を上述電場用電極材と適宜に組合わせて使用でき
る。この内本発明に好適な光電子放出材の種類は、一般
に少なくとも1部分が金網状のもの(特開昭61−17
8050号公報)、紫外線透過性物質例えばガラス材上
に光電子を放出し得る物質を薄膜状に付加したもの(特
願平2−295423号)、板あるいは曲面状のものを
1種又は2種類以上適宜組合わせて、光電子放出部に設
置したものである。光電子放出材と電極材の組合わせ
は、利用分野、装置規模、形状、構造などにより適宜決
めることができ、空間部に設置した場合に、後述の清浄
化空間部に存在する微粒子が光電子放出部に迅速に移動
できるものであれば何れでも良い。The type of photoelectron emitting material is a plate-shaped material, a pleat-shaped material, a wire mesh-shaped material (Japanese Patent Application Laid-Open No. 61-178050) as already proposed by the present inventor, and a protective film on the base material. With the addition of (Japanese Patent Application No. 1-155857),
A thin film (Japanese Patent Application No. 2-278123) and an ultraviolet-transparent substance (Japanese Patent Application No. 2-295423)
No.) can be used in an appropriate combination with the above electrode material for electric field. Among these, the kind of photoelectron emitting material suitable for the present invention is generally one in which at least one part is a wire mesh (Japanese Patent Laid-Open No. 61-17).
8050), an ultraviolet-transparent substance such as a glass material on which a substance capable of emitting photoelectrons is added in a thin film (Japanese Patent Application No. 2-295423), and one or more kinds of plate or curved surface. It is installed in the photoelectron emission unit in an appropriate combination. The combination of the photoelectron emitting material and the electrode material can be appropriately determined depending on the field of use, the scale of the device, the shape, the structure, etc. When installed in the space part, the fine particles present in the cleaning space part to be described later become Anything can be used as long as it can move quickly.
【0016】すなわち、光電子放出材又は電極の形状
は、清浄化空間部に存在する微粒子が、光電子放出部か
ら放出された光電子により荷電されるように、どちらか
一方が清浄化空間部に存在する微粒子が光電子放出部に
迅速に移動できるものであれば何れでも良い。このよう
な形状としては、通常金網状、線状、棒状、格子状、板
状、プリーツ状、曲面状等があり、これらを1種類ある
いは2種類以上適宜組合わせて用いることができる。こ
の内、金網状、棒状、線状、板状、格子状の形状のもの
を筒状で用いることが上記目的から好ましい。That is, as for the shape of the photoelectron emitting material or the electrode, one of them is present in the cleaning space so that the fine particles existing in the cleaning space are charged by the photoelectrons emitted from the photoelectron emitting part. Any particles may be used as long as the particles can move quickly to the photoelectron emitting portion. Such shapes are usually wire mesh, linear, rod-shaped, lattice-shaped, plate-shaped, pleated, curved, and the like, and these can be used alone or in combination of two or more kinds. Of these, it is preferable to use a wire mesh, rod, wire, plate, or lattice in a tubular shape for the above purpose.
【0017】光電子放出材と電極の位置と形状は、紫外
線源を囲み、紫外線源、光電子放出材、電極が一体化で
き、紫外線源から放出された紫外線が有効利用され、か
つ光電子の放出と該光電子による微粒子の荷電が効果的
に行えるように利用分野、装置規模、形状、効果、経済
性等を考慮して予備試験等により、決めることができ
る。例えば、棒(円筒)状の紫外線ランプを用いる場合
は、紫外線が円周方向に放射状に放出されるため、この
円周方向の放射状の紫外線を光電子放出材に出来るだけ
多く照射するほど光電子放出量が多くなる。The positions and shapes of the photoelectron emitting material and the electrodes surround the ultraviolet ray source, and the ultraviolet ray source, the photoelectron emitting material and the electrode can be integrated so that the ultraviolet ray emitted from the ultraviolet ray source can be effectively utilized and the photoelectron emission and the In order to effectively charge the fine particles by photoelectrons, it can be determined by a preliminary test or the like in consideration of the field of use, device scale, shape, effect, economical efficiency, and the like. For example, when using a rod-shaped (cylindrical) ultraviolet lamp, ultraviolet rays are emitted radially in the circumferential direction. Therefore, the more the radial radiation in the circumferential direction is applied to the photoelectron emitting material, the more the amount of photoelectron emission is increased. Will increase.
【0018】このため、図1の例では、紫外線ランプ1
1を先ず紫外線ランプ11の直径より大きい直径の円筒
状の石英ガラス(母材)12で囲み、該石英ガラス表面
に光電子放出材13として薄膜状のAuを付加した。更
に、その廻りに直径の更に大きい円筒状の金網14を電
極として囲み、紫外線ランプ11、光電子放出材13、
電極14を一体化している。図2の例では、紫外線ラン
プ21を先ず円筒状の目の粗い金網状の電極22で囲
み、更にその廻りに円筒状の金網23を囲み電子放出材
として用い、これらを一体化している。尚、ここでの金
網状光電子放出材23は、Cu−ZnにAuを薄膜状に
付加したものである。Therefore, in the example of FIG. 1, the ultraviolet lamp 1
First, 1 was surrounded by a cylindrical quartz glass (base material) 12 having a diameter larger than that of the ultraviolet lamp 11, and thin film Au was added as a photoelectron emitting material 13 to the surface of the quartz glass. Furthermore, a cylindrical metal net 14 having a larger diameter is surrounded by the electrode as an electrode, and the ultraviolet lamp 11, the photoelectron emitting material 13,
The electrode 14 is integrated. In the example of FIG. 2, the ultraviolet lamp 21 is first surrounded by a cylindrical wire mesh electrode 22, and a cylindrical wire mesh 23 is surrounded by the electrode 22, and is used as an electron emitting material to integrate them. The wire-mesh photoelectron emitting material 23 here is a thin film of Cu-Zn with Au added thereto.
【0019】図1で円筒状の電極14、図2で円筒状の
光電子放出材23は、いずれも金網状であり、これより
清浄化空間部の微粒子が容易に(拡散により)光電子放
出部に移動できる。また、光電子放出材への紫外線の照
射は電場において行うと、光電子放出材からの光電子発
生が効果的に起こる。電場の形成方法としては、荷電部
の形状、構造、適用分野或いは期待する効果(精度)等
によって適宜選択することが出来る。電場の強さは、共
存水分濃度や光電子放出材の種類等で適宜決めることが
出来、このことについては本発明者の別の発明がある。
電場の強さは、一般に0.1V/cm〜2KV/cmで
ある。Both the cylindrical electrode 14 in FIG. 1 and the cylindrical photoelectron emitting material 23 in FIG. 2 are in the shape of a wire mesh, so that the fine particles in the cleaning space can be easily (diffused) in the photoelectron emitting portion. You can move. Further, when the photoelectron emitting material is irradiated with ultraviolet rays in an electric field, photoelectrons are effectively generated from the photoelectron emitting material. The method of forming the electric field can be appropriately selected depending on the shape and structure of the charged portion, the field of application, the expected effect (accuracy), and the like. The strength of the electric field can be appropriately determined depending on the coexisting water concentration, the type of the photoelectron emitting material, etc., and there is another invention of the present inventor in this regard.
The strength of the electric field is generally 0.1 V / cm to 2 KV / cm.
【0020】光電子放出材と電極の間の距離は、これら
の間に電場が形成でき、光電子放出材への紫外線照射に
より光電子放出材からの光電子が微粒子に荷電を与える
ことができれば良く、近いほど印加電圧が低くて良いの
で好ましい。一般に20cm以内、好ましくは5cm以
内であるが装置規模、形状、利用分野などにより適宜に
決めることができる。The distance between the photoelectron emitting material and the electrode may be such that an electric field can be formed between them and the photoelectrons from the photoelectron emitting material can charge the fine particles by the irradiation of the photoelectron emitting material with ultraviolet rays. It is preferable because the applied voltage can be low. It is generally within 20 cm, preferably within 5 cm, but can be appropriately determined depending on the scale of the apparatus, shape, field of use, and the like.
【0021】[0021]
【実施例】以下、本発明の実施例を図面を用いて説明す
るが、本発明はこれに限定されるものではない。 実施例1 半導体工場のウェハ保管庫(図3)における空気清浄
を、図1に示した本発明の基本構成図の微粒子の荷電・
捕集ユニットを用い実施する場合を図1と図3を用い説
明する。図3の密閉空間(気体が流動せず、静止状態と
みなせる空間)であるウェハ保管庫の空気清浄は、ウェ
ハ保管庫の内側に設置された紫外線ランプ11、該ラン
プを囲む形状(円筒状)のガラス母材12上の光電子放
出材13、該光電子放出材13を囲む形状(円筒状)の
金網電極14より成る図1の微粒子の荷電・捕集ユニッ
トBにて実施される。Embodiments of the present invention will be described below with reference to the drawings, but the present invention is not limited thereto. Example 1 Air cleaning in a wafer storage (FIG. 3) of a semiconductor factory was performed by charging fine particles in the basic configuration diagram of the present invention shown in FIG.
A case where the collection unit is used will be described with reference to FIGS. 1 and 3. The air cleaning of the wafer storage, which is the closed space (space in which gas does not flow and can be regarded as a stationary state) in FIG. 3, is performed by the ultraviolet lamp 11 installed inside the wafer storage and the shape surrounding the lamp (cylindrical shape). 1 is composed of a photoelectron emission material 13 on the glass base material 12 and a wire mesh electrode 14 having a shape (cylindrical shape) surrounding the photoelectron emission material 13 and is carried out by the fine particle charging / collecting unit B in FIG.
【0022】すなわち、ウェハ保管庫中の微粒子(微粒
子状物質)16は図1の紫外線ランプ11が照射された
光電子放出材13から放出される光電子15により荷電
され、荷電微粒子となり、該荷電微粒子は荷電微粒子の
捕集材14に捕集され、ウェハの存在する清浄化空間部
(A)は高清浄化される。Bは、空間中微粒子の荷電・
捕集部であり、光電子放出部から光電子を放出させ、微
粒子を荷電させ、捕集(除去)する図1の微粒子の荷電
・捕集ユニットより成る。ここでの光電子放出材13
は、ガラス材表面に50ÅAuを薄膜状に付加したもの
である。このようにして、ウェハ保管庫中の微粒子(粒
子状物質)は捕集・除去され、ウェハ保管庫は清浄空気
となる。That is, the fine particles (fine particle substances) 16 in the wafer storage are charged by the photoelectrons 15 emitted from the photoelectron emitting material 13 irradiated with the ultraviolet lamp 11 in FIG. 1 to become charged fine particles, and the charged fine particles are The charged fine particles are collected by the collector 14, and the cleaning space (A) where the wafer exists is highly cleaned. B is the charge of fine particles in the space
The collecting unit is composed of the fine particle charging / collecting unit shown in FIG. 1 which emits photoelectrons from the photoelectron emitting unit to charge the fine particles and collect (remove) them. Photoelectron emission material 13 here
Is a thin film of 50ÅAu added to the surface of the glass material. In this way, the fine particles (particulate matter) in the wafer storage are collected and removed, and the wafer storage becomes clean air.
【0023】電極14は、光電子放出材13からの光電
子放出を電場で行うために設置している。すなわち、光
電子放出材13と電極14の間に電場を形成している
(光電子放出部)。微粒子の荷電は、電場において光電
子放出材13に紫外線照射することにより発生する光電
子15により効率よく実施される。ここでの電場の電圧
は、50V/cmである。また、荷電微粒子の捕集は、
電極14を用いて行っている。電極材は金網状のCu−
Zn材を金メッキして用い、光電子放出材より1cmの
位置に設置している。9,10は、夫々ウェハキャリャ
ー、ウェハを示す。本例において、ウェハ保管庫内の1
部に気流の攪拌を行うと微粒子除去速度が早くなること
から好ましい。その方法として、加温して温度差をつけ
る、機械的な攪拌等があり、適宜に使用できる。The electrode 14 is installed in order to perform photoelectron emission from the photoelectron emission material 13 in an electric field. That is, an electric field is formed between the photoelectron emitting material 13 and the electrode 14 (photoelectron emitting portion). The particles are efficiently charged by the photoelectrons 15 generated by irradiating the photoelectron emitting material 13 with ultraviolet rays in an electric field. The voltage of the electric field here is 50 V / cm. Also, the collection of charged fine particles is
This is performed using the electrode 14. The electrode material is a wire mesh Cu-
The Zn material is used after being plated with gold, and is installed at a position 1 cm from the photoelectron emitting material. Reference numerals 9 and 10 denote a wafer carrier and a wafer, respectively. In this example, 1 in the wafer storage
It is preferable to stir an air stream in the part because the removal rate of fine particles becomes faster. Examples of the method include heating and making a temperature difference, mechanical stirring, and the like, which can be appropriately used.
【0024】実施例2 図3に示したウェハ保管庫(清浄器)内部に図1に示し
た微粒子の荷電・捕集ユニットを設置し、下記試料ガス
を入れ紫外線照射並びに電圧の印加(荷電・捕集)を行
い、粒子測定器(パーティクルカウンター)を用い、微
粒子の残存率を調べた。 清浄器大きさ:10リットル 紫外線源:殺菌ランプ(棒状),6W 光電子放出材:円筒状石英ガラス表面に、薄膜状Au
(50Å)を付加したもの。 電極材:光電子放出材よりも2cm直径の長い円筒状の
金網(Cu−ZnをAuメッキしたもの)。 荷電微粒子の捕集材:電極材で兼用。 電場電圧:50V/cmExample 2 The particle charging / collecting unit shown in FIG. 1 was installed in the wafer storage (cleaner) shown in FIG. Collection was performed, and the residual rate of fine particles was examined using a particle measuring device (particle counter). Purifier size: 10 liters Ultraviolet source: Sterilizing lamp (rod), 6W Photoelectron emitting material: Cylindrical quartz glass surface, thin film Au
(50Å) added. Electrode material: Cylindrical wire mesh (Cu-Zn plated with Au) having a diameter 2 cm longer than that of the photoelectron emitting material. Collection material for charged fine particles: Also used as an electrode material. Electric field voltage: 50V / cm
【0025】微粒子の荷電・捕集ユニット:図1のごと
く、紫外線ランプ(殺菌ランプ)を円筒状の光電子放出
材で囲み、更にその廻りを円筒状の金網電極で囲んだも
の。試料ガス(入口ガス):表1のとおりParticle charging / collecting unit: As shown in FIG. 1, an ultraviolet lamp (sterilization lamp) is surrounded by a cylindrical photoelectron emitting material, and the surrounding area is surrounded by a cylindrical wire mesh electrode. Sample gas (inlet gas): as shown in Table 1
【表1】 [Table 1]
【0026】結果 0.1μm以上の微粒子濃度を測定器で測定した。結果
を表2に示す。Results A fine particle concentration of 0.1 μm or more was measured with a measuring instrument. Table 2 shows the results.
【表2】 尚、ブランクとして紫外線照射と電圧の印加なしの場
合の30分放置後の清浄器内の微粒子濃度を調べたとこ
ろ、初期濃度(入口濃度)に対し90%が認められた
(測定された)。[Table 2] As a blank, when the particle concentration in the purifier after leaving for 30 minutes in the case of no ultraviolet irradiation and no voltage application was examined, 90% of the initial concentration (inlet concentration) was recognized (measured).
【0027】実施例1では、微粒子の荷電・捕集ユニッ
トを清浄化空間に一台設置した場合であるが、適用分
野、装置規模、形状、効果等によっては複数台設置して
実施し得ることは言うまでもない。また、上述の例で
は、光電子放出材を紫外線源を囲む位置に設置した場合
を示したが、本発明者がすでに提案した紫外線源(紫外
線ランプ)の表面に薄膜状光電子放出材を付加した光電
子放出装置(特願平3−22685号)も同様に使用で
きる。この光電子放出装置を用いる場合は、該光電子放
出装置の廻りに上述の電極を設置し、一体化すれば良
い。In the first embodiment, one charging / collecting unit for fine particles is installed in the cleaning space, but a plurality of charging / collecting units may be installed depending on the application field, the scale of the apparatus, the shape, the effect, and the like. Needless to say. Further, in the above-mentioned example, the case where the photoelectron emitting material is installed at the position surrounding the ultraviolet source is shown, but the photoelectron in which the thin film photoelectron emitting material is added to the surface of the ultraviolet source (ultraviolet lamp) already proposed by the present inventor is shown. A discharging device (Japanese Patent Application No. 3-22685) can be used as well. When this photoelectron emission device is used, the above-mentioned electrodes may be installed around the photoelectron emission device and integrated.
【0028】[0028]
【発明の効果】本発明によれば、紫外線源を光電子放出
材及び電極で囲み一体化したことにより、 コンパクトな微粒子の荷電・捕集ユニット装置とな
った。 一体化において紫外線源を光電子放出材で囲み設置
したことにより、紫外線源からの放出紫外線がロスする
ことなく有効利用できるようになった。例えば、円周方
向に放射状に放出される紫外線に対し、該放出紫外線を
囲むように、光電子放出材を設置することで全ての方向
に放出される紫外線を光電子放出材に照射できた。 一体化において、光電子放出材の近傍に電極を設置
したことにより光電子放出材と電極間が近傍になったの
で、電場のための印加電圧が低くなった。又、電場は光
電子放出材と電極間という小空間であるので、清浄化空
間への電場の影響は無視し得た。According to the present invention, the ultraviolet ray source is surrounded by the photoelectron emitting material and the electrode and integrated, whereby a compact fine particle charging / collecting unit device is obtained. In the integration, the ultraviolet light source was surrounded by the photoelectron emitting material, so that the ultraviolet light emitted from the ultraviolet light source could be effectively used without loss. For example, by arranging the photoelectron emitting material so as to surround the emitted ultraviolet rays in a radial direction in the circumferential direction, the photoelectron emitting material can be irradiated with the ultraviolet rays emitted in all directions. In the integration, since the electrode was placed near the photoelectron emission material and the distance between the photoelectron emission material and the electrode became close, the applied voltage for the electric field became low. Since the electric field is a small space between the photoelectron emitting material and the electrode, the influence of the electric field on the cleaning space can be ignored.
【0029】 全ての方向に放出される紫外線が有効
利用されたので、紫外線源として紫外線ランプを用いる
場合、従来式に比べランプの使用本数が相当減少でき
た。これにより、使用電力が減少した。また、微粒子の
荷電・捕集器としての性能が向上した。 空間中の任意の場所に設置できるので、清浄化能力
が向上した。 従来式では、清浄化装置としての装置構造を制限す
るが、本荷電・捕集ユニットを用いればによりその制
限はない。すなわち、清浄化装置の設計の自由度が大と
なった。 清浄化装置において、初期設計値よりも清浄能力
(清浄速度)を改善したい場合、従来式では困難である
が、本法では本荷電・捕集ユニットを任意の場所に増設
できるので、清浄能力の改善が簡易にできる。 適用分野が広がり、実用性が向上した。Since the ultraviolet rays emitted in all directions are effectively used, the number of lamps used can be considerably reduced when the ultraviolet lamp is used as the ultraviolet source as compared with the conventional method. This reduced the power used. Also, the performance as a charge / collector of fine particles has been improved. Since it can be installed anywhere in the space, the cleaning ability is improved. In the conventional method, the device structure as a cleaning device is limited, but if the charging / collecting unit is used, it is not limited. That is, the degree of freedom in designing the cleaning device has increased. In the purifier, if you want to improve the cleaning capacity (cleaning speed) from the initial design value, it is difficult with the conventional method, but with this method, the charging / collecting unit can be installed at any location, so the cleaning capacity Can be easily improved. The field of application has expanded and practicality has improved.
【図1】(a)は本発明の微粒子の荷電・捕集ユニット
装置を示す概略構成図であり、(b)はその断面図であ
る。FIG. 1A is a schematic configuration diagram showing a fine particle charging / collecting unit device of the present invention, and FIG. 1B is a sectional view thereof.
【図2】本発明の他の微粒子の荷電・捕集ユニット装置
を示す概略構成図である。FIG. 2 is a schematic configuration diagram showing another particle charging / collecting unit device of the present invention.
【図3】本発明のユニットをウェハ保管庫の空気清浄に
用いた基本構成図である。FIG. 3 is a basic configuration diagram in which the unit of the present invention is used for air cleaning of a wafer storage.
【図4】公知のウェハ保管庫の空気清浄装置の基本構成
図である。FIG. 4 is a basic configuration diagram of a known air cleaning apparatus for a wafer storage.
2,11,21:紫外線ランプ、3,13,23:光電
子放出材、4,14,22:電極、7,15,24:光
電子、6,16:微粒子、9:ウェハキャリャー、1
0:ウェハ、12:石英ガラス2, 11, 21: ultraviolet lamp, 3, 13, 23: photoelectron emitting material, 4, 14, 22: electrode, 7, 15, 24: photoelectron, 6, 16: fine particles, 9: wafer carrier, 1
0: Wafer, 12: Quartz glass
Claims (2)
集ユニット装置において、紫外線源と光電子放出材及び
電極からなり、該紫外線源が棒状の紫外線ランプであ
り、該ランプを筒状の光電子放出材と金網電極で囲み一
体化してユニット化したことを特徴とする微粒子の荷電
・捕集ユニット装置。1. A unit for charging and collecting particles in a space by photoelectrons, comprising an ultraviolet source, a photoelectron emitting material and an electrode, wherein the ultraviolet source is a rod-shaped ultraviolet lamp, and the lamp emits a cylindrical photoelectron. A unit for charging and collecting fine particles, which is characterized by being surrounded by a material and a wire mesh electrode and integrated into a unit.
のガラス母材上に付加されるか、金網状であり、前記金
網電極の内側又は外側に配置されていることを特徴とす
る請求項1記載の微粒子の荷電・捕集ユニット装置。2. The photoelectron emission material is added on a glass base material of an ultraviolet-transparent material, or has a wire mesh shape, and is arranged inside or outside the wire mesh electrode. 1. A unit for charging and collecting fine particles according to 1.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP26128991A JPH0822393B2 (en) | 1991-09-13 | 1991-09-13 | Particle charging / collecting unit device |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP26128991A JPH0822393B2 (en) | 1991-09-13 | 1991-09-13 | Particle charging / collecting unit device |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0568910A JPH0568910A (en) | 1993-03-23 |
| JPH0822393B2 true JPH0822393B2 (en) | 1996-03-06 |
Family
ID=17359737
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP26128991A Expired - Fee Related JPH0822393B2 (en) | 1991-09-13 | 1991-09-13 | Particle charging / collecting unit device |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0822393B2 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6159421A (en) * | 1995-10-17 | 2000-12-12 | Ebara Corporation | Method of cleaning gases |
| JP3405439B2 (en) | 1996-11-05 | 2003-05-12 | 株式会社荏原製作所 | How to clean solid surfaces |
| US8092577B2 (en) | 2008-12-19 | 2012-01-10 | Steris Corporation | Method and apparatus for removing gaseous or vaporous sterilants from a medium |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61178050A (en) * | 1985-02-04 | 1986-08-09 | Ebara Corp | Method and apparatus for purifying air by irradiation of ultraviolet rays |
| JPS62244459A (en) * | 1986-04-16 | 1987-10-24 | Ebara Res Co Ltd | Method and apparatus for purifying air by irradiation of radioactive rays |
-
1991
- 1991-09-13 JP JP26128991A patent/JPH0822393B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0568910A (en) | 1993-03-23 |
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