EP0448929A1 - Suppression of particle generation in a modified clean room corona air ionizer - Google Patents
Suppression of particle generation in a modified clean room corona air ionizer Download PDFInfo
- Publication number
- EP0448929A1 EP0448929A1 EP91100551A EP91100551A EP0448929A1 EP 0448929 A1 EP0448929 A1 EP 0448929A1 EP 91100551 A EP91100551 A EP 91100551A EP 91100551 A EP91100551 A EP 91100551A EP 0448929 A1 EP0448929 A1 EP 0448929A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- corona
- air
- point
- air ionizer
- ionizer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01T—SPARK GAPS; OVERVOLTAGE ARRESTERS USING SPARK GAPS; SPARKING PLUGS; CORONA DEVICES; GENERATING IONS TO BE INTRODUCED INTO NON-ENCLOSED GASES
- H01T23/00—Apparatus for generating ions to be introduced into non-enclosed gases, e.g. into the atmosphere
Definitions
- the present invention relates to an improved corona air ionizer which eliminates microcontamination associated with conventional corona ionizers. Specifically, the invention provides for the elimination of ammonium nitrate buildup on the negative corona points and the elimination of bursts of submicron particles in corona ionizers by providing a stream of non-hydrogen-containing dry gas at the corona point during operation. Corona ionizers are commonly used in clean rooms, particularly clean rooms used in the manufacture of semiconductor devices.
- Corona air ionizers have historically had a reputation for generating particulate contamination, while being very effective at reducing electrostatic charges on surfaces. Controlling electrostatic discharge (ESD) and reducing the sedimentation rate of small submicron aerosol particles are described in the article by K. Dillenbeck entitled “Selection of Air Ionization Within the Cleanroom” in Proceedings of the 32nd Annual Technical Meeting of the IES, pp 387-392 and in the article by R.P. Donovan et al entitled "The Dependence of Particle Deposition Velocity on Surface Potential” in 1987 Proceedings of the IES, pp 473-478.
- ESD electrostatic discharge
- corona air ionizers usually generate large quantities of small (less than 0.1 ⁇ m) particles, primarily metal sputtered from the corona points themselves as noted in the article by B.Y.H. Liu et al entitled “Aerosol Charging and Neutralization and Electrostatic Discharge in Clean Rooms,” in J. Envir. Sci, March/April 1987, pp 42-46 and in the article by M. Suzuki et al entitled “Effectiveness of Air Ionization Systems in Clean Rooms" in Proceedings of the 34th Annual Technical Meeting of the IES, pp 405-412.
- Dispersive x-ray analysis ruled out tungsten as a major contributor to the remaining particles. Chemical analysis of the white precipitate on the negative points further showed it to be mostly NH4NO3, making it plausible that the particles are also NH4NO3. In addition to generating contamination, the precipitation necessitates replacing the points every month which contributes significantly to the cost of maintaining corona ionizers.
- Particulates generated in clean rooms are mostly charged. If electric fields are present arising from charged surfaces, a strong attraction is created between the particles and the corresponding apparatus charged surfaces. The described phenomena is the primary cause for the anomalously large deposition rates seen in manufacturing at small particle sizes.
- triboelectric charging of semiconductor wafers, wafer boats, equipment, people and work surfaces result in electrostatic discharge events which can damage the wafers both electrically, by breaking down insulating layers and fusing conductors, and through the ablation of small particles from the surfaces involved in the discharge.
- a technique that has been employed to reduce these electrostatic affects is to neutralize the surfaces of the products and tools on a manufacturing line by adding air ions of both positive and negative polarities to the output of laminar flow HEPA filters, thereby rendering the air sufficiently conductive to neutralize the surface charges.
- typical electric fields produced by ungrounded wafers or containers are a few hundred to a few thousand volts per centimeter.
- the deposition rates for particles out of class 100 air is roughly 100 times lower for environments that incorporate air ionization than for those without air ionization as noted in the article by R. Welker entitled "Equivalence Between Surface Contamination Rates and Class 100 Conditions", 1988 Proceedings, IES, pp 449-454. The effect is attributed to the neutralization effect of the injected charge in the air on the excess surface charges.
- Ammonium nitrate is a compound of nitrogen, hydrogen and oxygen. It is a high-energy compound and can ordinarily be formed only in a high energy density environment such as a high temperature gas reactor, lightning discharge, or in the present case, corona discharge. If the particles are ammonium nitrate, then the formation of particles requires a source of hydrogen. The most plausible source of hydrogen is atmospheric water vapor. It follows that if the corona discharge is made to occur in a sufficiently dry gas environment, no ammonium nitrate will be generated.
- the corona points of a conventional corona ionizer are disposed in a stream of non-hydrogen-containing dry gas which will not corrode the corona points and will not form water vapor, for instance by placing the corona points inside a closed end tube with a clean non-hydrogen-containing dry gas, such as dry air, oxygen, carbon dioxide, nitrogen, argon or helium, flowing through the corona points.
- a clean non-hydrogen-containing dry gas such as dry air, oxygen, carbon dioxide, nitrogen, argon or helium
- a principal object of the present invention is therefore, the provision of an apparatus for suppressing particle generation in a corona air ionizer.
- Another object of the invention is the provision of eliminating ammonium nitrate particles usually created in corona ionizers by the use of a stream of non-hydrogen-containing dry gas.
- corona point 10 of a conventional ionizer is disposed inside a closed-end tube 12.
- the corona point is connected to a high voltage power source for generating ions by corona discharge.
- Clean non-hydrogen-containing dry gas which will not corrode the corona points and will not form water vapor, preferably dry air, oxygen, carbon dioxide, nitrogen, argon or helium, enters from conduit 14 into tube 12.
- the open end of the tube is positioned in front (above in the figure) of the corona point so that the ions generated by the discharge are carried out through the opening with the stream of non-hydrogen-containing dry gas.
- Oxygen and water vapor from the surrounding ambient air are prevented from approaching the corona points by the outwardly flowing gas.
- the outflowing ions mix with the ambient air, providing an ionization essentially indistinguishable from the unmodified ionizer operating in the ambient air.
- a bipolar DC corona ionizer Semtronics, Inc. Model 2001, was modified.
- the ionizer consists of a 2m long plastic extrusion (formed by joining two 1m lengths together end to end) whose cross-section is shaped in the form of the Greek letter capital sigma " ⁇ ", with the positive points spaced at 30 cm intervals along the middle of the upper groove and the negative points are similarly positioned in the other groove in a staggered relation so that each positive point is 15 cm from the closest negative point.
- the bar hangs horizontally, with the grooves facing sideways.
- the left-hand piece of the ionizer was left unmodified and the right-hand piece was modified as shown in Figure 2. In operation, the entire ionizer will be modified as described below.
- Both right-side extruded channels are covered, for example with PVC tape 20.
- a hole of approximately 1 cm diameter is cut in front of each corona point.
- the region below the tape 20 is continuously flushed with a clean non-hydrogen-containing dry gas which will not corrode the corona point and will not form water vapor, such as dry air, oxygen, carbon dioxide, nitrogen, argon or helium, via a perforated tube 24, made for example of Teflon, with a high-efficiency in-line filter (not shown).
- the corona points are manufactured of pure tungsten.
- the corona points are connected to a high voltage power source (not shown) for generating ions by corona discharge.
- the sleeves 22 must be kept away from the discharge region to avoid creating particles arising from erosion of the sleeves.
- the sleeves are preferably more than 4 mm from the tips of the corona points 26.
- the bar was hung 60 cm from a clean room wall, in unobstructed 90 cm/s vertical air flow about 20 cm below ceiling HEPA filters.
- Results showed that while the control air-immersed corona points had the characteristic white NH4NO3 deposits, there was no visible contamination of the dry gas immersed point.
- An important aspect of the invention is that much pre-existing air ionization equipment is capable of being upgraded for use in clean rooms producing semiconductor devices with submicron features; where the use of such an ionizer has previously been precluded by the particles generated.
- the modification is simple, inexpensive and does not require any change in the operation of the system.
Abstract
Description
- The present invention relates to an improved corona air ionizer which eliminates microcontamination associated with conventional corona ionizers. Specifically, the invention provides for the elimination of ammonium nitrate buildup on the negative corona points and the elimination of bursts of submicron particles in corona ionizers by providing a stream of non-hydrogen-containing dry gas at the corona point during operation. Corona ionizers are commonly used in clean rooms, particularly clean rooms used in the manufacture of semiconductor devices.
- Corona air ionizers have historically had a reputation for generating particulate contamination, while being very effective at reducing electrostatic charges on surfaces. Controlling electrostatic discharge (ESD) and reducing the sedimentation rate of small submicron aerosol particles are described in the article by K. Dillenbeck entitled "Selection of Air Ionization Within the Cleanroom" in Proceedings of the 32nd Annual Technical Meeting of the IES, pp 387-392 and in the article by R.P. Donovan et al entitled "The Dependence of Particle Deposition Velocity on Surface Potential" in 1987 Proceedings of the IES, pp 473-478. Unfortunately, corona air ionizers usually generate large quantities of small (less than 0.1 µm) particles, primarily metal sputtered from the corona points themselves as noted in the article by B.Y.H. Liu et al entitled "Aerosol Charging and Neutralization and Electrostatic Discharge in Clean Rooms," in J. Envir. Sci, March/April 1987, pp 42-46 and in the article by M. Suzuki et al entitled "Effectiveness of Air Ionization Systems in Clean Rooms" in Proceedings of the 34th Annual Technical Meeting of the IES, pp 405-412.
- Recently, an article by K.D. Murray et al entitled "Ozone and Small Particles Production by Steady State DC Hood Ionization: An Evaluation" in 1989 EOS/ESD Symposium Proceedings, pp. 18-22 and an article by K.D. Murray et al entitled "Hood Ionization in Semiconductor Wafer Processing: An Evaluation" in 1988 EOS/ESD Symposium Proceedings, pp 195-200, have shown that proper point design and material selection, in particular the use of plain tungsten corona points instead of thoriated tungsten corona points and careful control of the tip shape, can reduce the sputtered metal to insignificant levels, and have suggested that the major remaining source of contamination is ammonium nitrate (NH₄NO₃) precipitated onto the negative corona points from the ambient air. Dispersive x-ray analysis ruled out tungsten as a major contributor to the remaining particles. Chemical analysis of the white precipitate on the negative points further showed it to be mostly NH₄NO₃, making it plausible that the particles are also NH₄NO₃. In addition to generating contamination, the precipitation necessitates replacing the points every month which contributes significantly to the cost of maintaining corona ionizers.
- Experience has shown that the quantity of particles present often vary from none to tens of thousands of particles per cubic foot in a short time period. The highly intermittent character makes the emission episodes difficult to analyze. The problem is compounded of the lack of control over several relevant variables, such as humidity and temperature.
- Particulates generated in clean rooms are mostly charged. If electric fields are present arising from charged surfaces, a strong attraction is created between the particles and the corresponding apparatus charged surfaces. The described phenomena is the primary cause for the anomalously large deposition rates seen in manufacturing at small particle sizes. In addition, triboelectric charging of semiconductor wafers, wafer boats, equipment, people and work surfaces result in electrostatic discharge events which can damage the wafers both electrically, by breaking down insulating layers and fusing conductors, and through the ablation of small particles from the surfaces involved in the discharge.
- A technique that has been employed to reduce these electrostatic affects is to neutralize the surfaces of the products and tools on a manufacturing line by adding air ions of both positive and negative polarities to the output of laminar flow HEPA filters, thereby rendering the air sufficiently conductive to neutralize the surface charges. For example, typical electric fields produced by ungrounded wafers or containers are a few hundred to a few thousand volts per centimeter. The deposition rates for particles out of class 100 air is roughly 100 times lower for environments that incorporate air ionization than for those without air ionization as noted in the article by R. Welker entitled "Equivalence Between Surface Contamination Rates and Class 100 Conditions", 1988 Proceedings, IES, pp 449-454. The effect is attributed to the neutralization effect of the injected charge in the air on the excess surface charges.
- Ammonium nitrate is a compound of nitrogen, hydrogen and oxygen. It is a high-energy compound and can ordinarily be formed only in a high energy density environment such as a high temperature gas reactor, lightning discharge, or in the present case, corona discharge. If the particles are ammonium nitrate, then the formation of particles requires a source of hydrogen. The most plausible source of hydrogen is atmospheric water vapor. It follows that if the corona discharge is made to occur in a sufficiently dry gas environment, no ammonium nitrate will be generated.
- In the present invention, the corona points of a conventional corona ionizer are disposed in a stream of non-hydrogen-containing dry gas which will not corrode the corona points and will not form water vapor, for instance by placing the corona points inside a closed end tube with a clean non-hydrogen-containing dry gas, such as dry air, oxygen, carbon dioxide, nitrogen, argon or helium, flowing through the corona points.
- A principal object of the present invention is therefore, the provision of an apparatus for suppressing particle generation in a corona air ionizer.
- Another object of the invention is the provision of eliminating ammonium nitrate particles usually created in corona ionizers by the use of a stream of non-hydrogen-containing dry gas.
- Further objects of the present invention will become more clearly apparent when the following description is read in conjunction with the accompanying drawings.
- Fig. 1
- is a schematic representation, in section, of the corona points of corona ionizers in accordance with the present invention; and
- Fig. 2
- is a cross-section view of a modified end of a corona ionizer.
- Referring now to the figures and to Fig. 1 in
particular corona point 10 of a conventional ionizer is disposed inside a closed-end tube 12. The corona point is connected to a high voltage power source for generating ions by corona discharge. Clean non-hydrogen-containing dry gas which will not corrode the corona points and will not form water vapor, preferably dry air, oxygen, carbon dioxide, nitrogen, argon or helium, enters fromconduit 14 intotube 12. The open end of the tube is positioned in front (above in the figure) of the corona point so that the ions generated by the discharge are carried out through the opening with the stream of non-hydrogen-containing dry gas. Oxygen and water vapor from the surrounding ambient air are prevented from approaching the corona points by the outwardly flowing gas. The outflowing ions mix with the ambient air, providing an ionization essentially indistinguishable from the unmodified ionizer operating in the ambient air. - In a preferred embodiment of the invention, a bipolar DC corona ionizer, Semtronics, Inc. Model 2001, was modified. The ionizer consists of a 2m long plastic extrusion (formed by joining two 1m lengths together end to end) whose cross-section is shaped in the form of the Greek letter capital sigma "Σ", with the positive points spaced at 30 cm intervals along the middle of the upper groove and the negative points are similarly positioned in the other groove in a staggered relation so that each positive point is 15 cm from the closest negative point. In operation, the bar hangs horizontally, with the grooves facing sideways. During testing, in order to provide a control, the left-hand piece of the ionizer was left unmodified and the right-hand piece was modified as shown in Figure 2. In operation, the entire ionizer will be modified as described below.
- Both right-side extruded channels are covered, for example with
PVC tape 20. A hole of approximately 1 cm diameter is cut in front of each corona point. Asleeve 22, preferably one cm long, and made from 0.5 inch OD Tygon tubing, is inserted into the hole to prevent moist air from being entrained into the region of the corona point by turbulence. The region below thetape 20 is continuously flushed with a clean non-hydrogen-containing dry gas which will not corrode the corona point and will not form water vapor, such as dry air, oxygen, carbon dioxide, nitrogen, argon or helium, via aperforated tube 24, made for example of Teflon, with a high-efficiency in-line filter (not shown). The corona points are manufactured of pure tungsten. The corona points are connected to a high voltage power source (not shown) for generating ions by corona discharge. - The
sleeves 22 must be kept away from the discharge region to avoid creating particles arising from erosion of the sleeves. The sleeves are preferably more than 4 mm from the tips of thecorona points 26. The bar was hung 60 cm from a clean room wall, in unobstructed 90 cm/s vertical air flow about 20 cm below ceiling HEPA filters. - Results showed that while the control air-immersed corona points had the characteristic white NH₄NO₃ deposits, there was no visible contamination of the dry gas immersed point.
- After eliminating sputtered metal particles by proper corona point design, the residual particle generation from a commercially available DC air ionizer is highly dependent on humidity in the immediate vicinity of the corona discharge. A modification to the ionizer design to exclude water vapor and other hydrogen sources essentially eliminated a major source of contamination.
- With the water vapor excluded, there is no hydrogen source from which to make ammonia, and so the particle generation ceases.
- The elimination of all hydrogen sources from the vicinity of the corona point prevents the formation of ammonia thereby suppressing particle generation.
- An important aspect of the invention is that much pre-existing air ionization equipment is capable of being upgraded for use in clean rooms producing semiconductor devices with submicron features; where the use of such an ionizer has previously been precluded by the particles generated. The modification is simple, inexpensive and does not require any change in the operation of the system.
Claims (7)
- A corona air ionizer comprising:
a housing (12, 20);
a corona point (10, 26) disposed in said housing;
a high voltage source coupled to said corona point;
feed means (14, 24) coupled to said housing for causing a stream of non-hydrogen-containing dry gas to flow past said corona point (10, 26) for causing ions generated by corona discharge to be carried out of said housing away from said corona point. - A corona air ionizer as set forth in claim 1, wherein said housing comprises a closed-end tube (12).
- A corona air ionizer as set forth in claim 1, further comprising perforated cover means (20) coupled to said housing and disposed in proximity to said corona point (26) and said feed means (24) whereby ions generated by corona discharge pass through said perforation.
- A corona air ionizer as set forth in claim 3, further comprising sleeve means (22) disposed through said perforation for channeling ions generated by corona discharge through said sleeve means.
- A corona air ionizer as set forth in anyone of the claims 1 to 4, wherein said dry gas is selected from the group consisting of dry air, oxygen, carbon dioxide, nitrogen, argon and helium.
- A method of suppressing particle generation in a corona air ionizer having a corona point comprising the step of flowing a stream of non-hydrogen-containing dry gas past said corona point.
- A method as set forth in claim 6, wherein said dry gas is selected from the group consisting of dry air, oxygen, carbon dioxide, nitrogen, argon and helium.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US49988090A | 1990-03-27 | 1990-03-27 | |
US499880 | 1990-03-27 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0448929A1 true EP0448929A1 (en) | 1991-10-02 |
EP0448929B1 EP0448929B1 (en) | 1995-08-02 |
Family
ID=23987129
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP91100551A Expired - Lifetime EP0448929B1 (en) | 1990-03-27 | 1991-01-18 | Suppression of particle generation in a modified clean room corona air ionizer |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP0448929B1 (en) |
JP (1) | JP2838856B2 (en) |
DE (1) | DE69111651T2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995007175A1 (en) * | 1993-09-10 | 1995-03-16 | The University Of Tennessee Research Corporation | Electrostatic charging apparatus and method |
FR2769758A1 (en) * | 1997-10-14 | 1999-04-16 | Thomas Sebald | HIGH VOLTAGE GENERATION DEVICE FOR GAS IONIZATION |
CN104056721A (en) * | 2009-04-24 | 2014-09-24 | 伊利诺斯工具制品有限公司 | Clean Corona Gas Ionization For Static Charge Neutralization |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3004951U (en) * | 1994-06-03 | 1994-12-06 | 株式会社山口工業 | Automotive paint surface pretreatment equipment |
JP2880427B2 (en) * | 1995-06-29 | 1999-04-12 | 株式会社テクノ菱和 | Air ionization apparatus and air ionization method |
RU2598098C2 (en) * | 2008-04-29 | 2016-09-20 | Закрытое Акционерное Общество "Техмаш" | Air ioniser |
WO2016134701A1 (en) | 2015-02-24 | 2016-09-01 | Estion Technologies Gmbh | X-ray source for ionising of gases |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2202625A5 (en) * | 1972-10-06 | 1974-05-03 | Anvar |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS52132329A (en) * | 1976-04-30 | 1977-11-07 | Jirou Asahina | High voltage ionizing apparatus |
JPS553146A (en) * | 1978-06-21 | 1980-01-10 | Minoru Watanabe | Air ion generator |
US4333123A (en) * | 1980-03-31 | 1982-06-01 | Consan Pacific Incorporated | Antistatic equipment employing positive and negative ion sources |
DE3331804A1 (en) * | 1983-09-02 | 1985-04-04 | Gesellschaft für Ionentechnik mbH, 7032 Sindelfingen | DEVICE FOR GENERATING NEGATIVE IONS |
JPS60241690A (en) * | 1984-02-13 | 1985-11-30 | バイオメツド、エレクトロニツク、ゲゼルシヤフト、ミツト、ベシユレンクテル、ハフツング、ウント、コンパニ−、メデイツイ−ニシエル、ゲレ−テバウ、コマンデイ−トゲゼルシヤフト | Ionized chamber for ionizing gas oxygen |
JPS6240459A (en) * | 1985-08-16 | 1987-02-21 | Toshiba Corp | Plate cleaner |
JPS63127155A (en) * | 1986-11-17 | 1988-05-31 | Masahiko Tsuchiya | Thin film analyzer |
-
1991
- 1991-01-18 DE DE1991611651 patent/DE69111651T2/en not_active Expired - Fee Related
- 1991-01-18 EP EP91100551A patent/EP0448929B1/en not_active Expired - Lifetime
- 1991-02-22 JP JP3048824A patent/JP2838856B2/en not_active Expired - Fee Related
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2202625A5 (en) * | 1972-10-06 | 1974-05-03 | Anvar |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5592357A (en) * | 1992-10-09 | 1997-01-07 | The University Of Tennessee Research Corp. | Electrostatic charging apparatus and method |
WO1995007175A1 (en) * | 1993-09-10 | 1995-03-16 | The University Of Tennessee Research Corporation | Electrostatic charging apparatus and method |
FR2769758A1 (en) * | 1997-10-14 | 1999-04-16 | Thomas Sebald | HIGH VOLTAGE GENERATION DEVICE FOR GAS IONIZATION |
DE19745316C2 (en) * | 1997-10-14 | 2000-11-16 | Thomas Sebald | Device for generating high voltage for the ionization of gases |
CN104056721A (en) * | 2009-04-24 | 2014-09-24 | 伊利诺斯工具制品有限公司 | Clean Corona Gas Ionization For Static Charge Neutralization |
CN104056721B (en) * | 2009-04-24 | 2017-07-28 | 伊利诺斯工具制品有限公司 | The clean corona gas ionization neutralized for electrostatic |
Also Published As
Publication number | Publication date |
---|---|
DE69111651D1 (en) | 1995-09-07 |
JPH04223085A (en) | 1992-08-12 |
JP2838856B2 (en) | 1998-12-16 |
DE69111651T2 (en) | 1996-04-18 |
EP0448929B1 (en) | 1995-08-02 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US5116583A (en) | Suppression of particle generation in a modified clean room corona air ionizer | |
KR100208641B1 (en) | Air ionizing apparatus and method | |
JP6374582B2 (en) | Gas ionizer, method of generating an ionized gas stream, and method of converting a cloud of free electrons to negative ions in a corona discharge ionizer | |
US7397647B2 (en) | Ionized gas current emission type dust-free ionizer | |
EP2422219B1 (en) | Clean corona gas ionization for static charge neutralization | |
US4827371A (en) | Method and apparatus for ionizing gas with point of use ion flow delivery | |
US20090176431A1 (en) | Method of forming a corona electrode substantially of chemical vapor deposition silicon carbide and a method of ionizing gas using the same | |
US5249094A (en) | Pulsed-DC ionizer | |
EP0448929B1 (en) | Suppression of particle generation in a modified clean room corona air ionizer | |
JPH04503422A (en) | Improvements in corona discharge equipment for removing harmful substances generated by corona discharge | |
JP2013519978A (en) | Separation of contaminants from gaseous ions in a corona discharge ionization bar. | |
JPH0817171B2 (en) | Plasma generator and etching method using the same | |
Hobbs et al. | Suppression of particle generation in a modified clean room corona air ionizer | |
Davidson et al. | Chemical vapor deposition in the corona discharge of electrostatic air cleaners | |
Islamov et al. | Erosion and lifetime of tungsten, gold, and nichrome wire anodes in an ultracorona in air | |
Ramasamy et al. | Current-voltage characteristics of a non-transferred plasma spray torch | |
EP1164821A2 (en) | Static eliminator employing DC-biased corona with extended structure | |
JPH0479180A (en) | Ionized gas generating device | |
BEDOUI | Microscopic Modeling Barrier | |
White | The role of corona discharge in the electrical precipitation process | |
JP3078819B2 (en) | Ion generator | |
Jeong et al. | A study on the electrohydrodynamic flow in a rectangular impactor with positive corona discharge | |
Imazono et al. | Dual Jet Ionizer for Manufacturing Semiconductor Devices | |
JPH10208898A (en) | Air blowoff port to neutralize electrified article | |
Chutov et al. | Computer modeling of pulsing discharges in dielectric cell with dust particles |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): DE FR GB |
|
17P | Request for examination filed |
Effective date: 19911219 |
|
17Q | First examination report despatched |
Effective date: 19920224 |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): DE FR GB |
|
REF | Corresponds to: |
Ref document number: 69111651 Country of ref document: DE Date of ref document: 19950907 |
|
ET | Fr: translation filed | ||
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 19960103 Year of fee payment: 6 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 19960126 Year of fee payment: 6 |
|
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
26N | No opposition filed | ||
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 19961220 Year of fee payment: 7 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FR Effective date: 19970930 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DE Effective date: 19971001 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 19980118 |
|
GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 19980118 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R081 Ref document number: 69111651 Country of ref document: DE Owner name: GLOBALFOUNDRIES INC., KY Free format text: FORMER OWNER: INTERNATIONAL BUSINESS MACHINES CORPORATION, ARMONK, NY, US Ref country code: DE Ref legal event code: R082 Ref document number: 69111651 Country of ref document: DE Representative=s name: RICHARDT PATENTANWAELTE PARTG MBB, DE Ref country code: DE Ref legal event code: R081 Ref document number: 69111651 Country of ref document: DE Owner name: GLOBALFOUNDRIES INC., KY Free format text: FORMER OWNER: INTERNATIONAL BUSINESS MACHINES CORPORATION, ARMONK, N.Y., US |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R082 Ref document number: 69111651 Country of ref document: DE Representative=s name: RICHARDT PATENTANWAELTE PARTG MBB, DE Ref country code: DE Ref legal event code: R081 Ref document number: 69111651 Country of ref document: DE Owner name: GLOBALFOUNDRIES INC., KY Free format text: FORMER OWNER: GLOBALFOUNDRIES US 2 LLC (N.D.GES.DES STAATES DELAWARE), HOPEWELL JUNCTION, N.Y., US |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: TP Owner name: GLOBALFOUNDRIES INC., GB Effective date: 20160829 |