US20020054839A1 - Method and apparatus for efficient surface generation of pure O3 - Google Patents

Method and apparatus for efficient surface generation of pure O3 Download PDF

Info

Publication number
US20020054839A1
US20020054839A1 US10/034,084 US3408401A US2002054839A1 US 20020054839 A1 US20020054839 A1 US 20020054839A1 US 3408401 A US3408401 A US 3408401A US 2002054839 A1 US2002054839 A1 US 2002054839A1
Authority
US
United States
Prior art keywords
plasma
quencher
ozone
chamber
plasma source
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.)
Abandoned
Application number
US10/034,084
Inventor
Yee Chen
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.)
Chen Laboratories
Original Assignee
Chen Laboratories
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 Chen Laboratories filed Critical Chen Laboratories
Priority to US10/034,084 priority Critical patent/US20020054839A1/en
Publication of US20020054839A1 publication Critical patent/US20020054839A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B13/00Oxygen; Ozone; Oxides or hydroxides in general
    • C01B13/10Preparation of ozone
    • C01B13/11Preparation of ozone by electric discharge
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B13/00Oxygen; Ozone; Oxides or hydroxides in general
    • C01B13/10Preparation of ozone
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2201/00Preparation of ozone by electrical discharge
    • C01B2201/90Control of the process

Definitions

  • the present invention relates generally to a methodology of generating ozone, and more particularly, to a method and apparatus for efficient surface generation of high concentration ozone and liquid ozone.
  • O 3 ozone
  • a majority of the known state-of-the-art O 3 generation is accomplished through corona discharge, which has a yield on the order of around ten to fifteen percent (10-15%) maximum and at a low generation rate.
  • Usage of O 3 has typically been limited to a low concentration (e.g., less than fifteen percent ( ⁇ 15%) and the generating of O 3 constrained to being generated at the point-of-use.
  • UV ozone generation Another method of ozone generation is UV ozone generation, which has an even lower concentration yield as compared to electric discharge ozone generation.
  • a third and less popular method is electrolytic ozone generation. With electrolytic ozone generation, aqueous solutions of sulfuric or perchloric acid are electrolyzed with extremely high anodic current densities. In the later instance, oxygen (O 2 ) and, in the case of sulfuric acid solutions, peroxydisulfuric acid, H 2 S 2 O 8 , are by-products.
  • an apparatus for generating ozone includes a chamber and a plasma source.
  • the plasma source couples to the chamber and produces oxygen plasma from a supply of oxygen.
  • the plasma includes at least a mixture of O and O 2 species.
  • a quencher is disposed within the chamber proximate an output of the plasma source for facilitating ozone generation from the mixture of O and O 2 species.
  • a technical advantage provided by the embodiments of the present disclosure is the generation of high concentration O 3 at the point-of-use or location other than the point-of-use.
  • the present embodiments provide the ability for achieving a substantially limitless scalable production rate and volume of high concentration O 3 .
  • FIG. 1 illustrates a schematic view of an apparatus for surface generation of ozone according to an embodiment of the present disclosure
  • FIG. 2 illustrates a schematic view of an apparatus for surface generation of ozone according to another embodiment of the present disclosure
  • FIG. 3 illustrates a schematic view of an apparatus for surface generation of ozone according to another embodiment
  • FIG. 4 illustrates a cross sectional view of a quencher of FIG. 3 in greater detail
  • FIGS. 5A and 5B illustrate a top view and a cross section view of a portion of the quencher of FIG. 4;
  • FIG. 6 illustrates a block diagram view of a system apparatus for processing media utilizing the method and apparatus for surface generation of ozone of the present disclosure.
  • an apparatus 10 for generating ozone includes a chamber 12 , such as a vacuum chamber or other suitable chamber.
  • a plasma source 14 couples to the chamber 12 for producing oxygen plasma 16 from a supply of oxygen 18 .
  • the plasma 16 includes at least a mixture of O and O 2 species.
  • a quencher 20 is disposed within the chamber 12 proximate an output of the plasma source 14 for facilitating ozone generation from the mixture of O and O 2 species.
  • the plasma source 14 includes an R.F. plasma source, a microwave source, or other suitable plasma sources. Electrical power is supplied to plasma source 14 as indicated by reference numeral 22 .
  • the quencher 20 includes a quenching surface located down-stream of the plasma source within a prescribed region 17 of the oxygen plasma 16 , such as in the plasma plume.
  • the oxygen plasma flows across the quenching surface to generate ozone.
  • the quenching surface includes a plurality of quenching surfaces.
  • the plurality of quenching surfaces include a plurality of flow channels 24 having inputs 26 and outputs 28 , the inputs 26 being disposed proximate the output of the plasma source 14 .
  • System apparatus 10 further includes a controller 30 .
  • Controller 30 includes any suitable programmable controller or computer for use in controlling various process parameters of the present method and apparatus. Process parameters are selected according to a prescribed process parameter window for a given ozone generation application (or for generation of a poly-atomic molecular form of a prescribed element). Controller 30 is programmed for performing desired functions as discussed herein. Programming may be accomplished using techniques well known in the art, thus not discussed further herein.
  • Controller 30 provides appropriate control signals for supply gas control 32 , temperature control 34 , plasma control 36 , and vacuum pump control 38 .
  • Vacuum pump 40 provides a desired vacuum within chamber 12 , as may be required for a given application.
  • Controller 30 provides additional control signals, as may be needed, for control of additional parameters of a prescribed process window.
  • the apparatus 10 for generating ozone further includes means for controlling a temperature of the quencher in a prescribed manner for producing a desired form of liquid-phase or gas-phase ozone.
  • Temperature control includes providing a thermal channel 42 in communication with the quencher 20 suitable for passage of a prescribed coolant through the thermal channel.
  • the temperature control further includes controlling a flow rate of coolant through the thermal channel, such as, with a controllable flow valve or regulator (not shown).
  • Controller 30 provides a temperature control signal 34 , which may be used for controlling the flow valve or regulator, as appropriate.
  • the coolant may include liquid nitrogen, liquid helium, liquid oxygen, or other suitable coolant.
  • FIG. 1 an enlarged view 50 of a portion of a flow channel 24 is shown.
  • the enlarged view 50 illustrates several layers of adsorbed O 2 on the quencher surface 52 of a flow channel 24 .
  • the layers of adsorbed O 2 are characterized by an inner layer 54 , intermediate layer (or layers) 56 , and an outer layer 58 , as discussed further herein below.
  • O from the mixture of O 2 and O collide with the O 2 from an outer layer 58 to produce O 3 .
  • O 3 in the liquid phase 60 migrates to the quencher surface 52 (or O 3 in the gas phase 62 flows within channel 24 ) to the output 28 of the respective flow channel 24 .
  • the method includes providing a chamber, such as a vacuum chamber or other suitable chamber.
  • the method further includes providing a plasma source coupled to the chamber for producing oxygen plasma from a supply of oxygen.
  • the plasma includes at least a mixture of O and O 2 species.
  • a quencher is disposed within the chamber proximate an output of the plasma source for facilitating ozone generation from the mixture of O and O 2 species.
  • the plasma source includes an R.F. plasma source, a microwave source, or other suitable source.
  • Providing the quencher includes providing a quenching surface located down-stream of the plasma source within a prescribed region of the oxygen plasma, wherein the oxygen plasma flows across the quenching surface to generate ozone.
  • the quenching surface includes a plurality of quenching surfaces.
  • the plurality of quenching surfaces include a plurality of flow channels having inputs and outputs, the inputs disposed proximate the output of the plasma source.
  • the method further includes controlling a temperature of the quencher in a prescribed manner for producing a desired form of liquid-phase or gas-phase ozone.
  • Controlling the temperature of the quencher includes providing a thermal channel in communication with the quencher suitable for passage of a prescribed coolant through the thermal channel.
  • Controlling the temperature further includes controlling a flow rate of coolant through the thermal channel.
  • the coolant includes liquid nitrogen, liquid helium, liquid oxygen, or other suitable coolant.
  • a method of generating ozone includes supplying oxygen to a plasma source; igniting and producing an oxygen plasma with the plasma source, and directing the oxygen plasma for movement over a quenching surface of a quencher.
  • the oxygen plasma contains a mixture of O and O 2 .
  • the quenching surface is positioned down-stream of the plasma source within a prescribed region of the oxygen plasma.
  • the oxygen plasma flows across the quenching surface to facilitate ozone generation from the mixture of O and O 2 .
  • the quenching surface includes a plurality of flow channels disposed within the quencher, the flow channels having inputs and outputs. The flow channel inputs are arranged proximate an output of the plasma source.
  • the method further includes controlling a temperature of the quenching surface in a prescribed manner for producing a desired form of liquid-phase or gas-phase ozone.
  • the temperature of the quenching surface may also be regulated. Regulating the temperature includes controlling the flow rate of a coolant flowing through a cooling channel disposed in the quencher.
  • the coolant may include liquid nitrogen, liquid helium, liquid oxygen, or other suitable coolant.
  • the present embodiments further include an apparatus for generating a polyatomic form of a prescribed element.
  • the apparatus includes a chamber, a plasma source coupled to the chamber, and a quencher.
  • the plasma source produces plasma of the prescribed element from a supply of the element in a gaseous state. Accordingly, the plasma includes at least a mixture of single atomic, double atomic and polyatomic species of the prescribed element.
  • the quencher is disposed within the chamber proximate an output of the plasma source.
  • the quencher facilitates generation of the polyatomic form of the prescribed element from the mixture of single atomic, double atomic and polyatomic species of the prescribed element.
  • the plasma source includes an R.F. plasma source, a microwave source, or other suitable plasma source.
  • the quencher includes a quenching surface located down-stream of the plasma source within a prescribed region of the plasma. The plasma flows across the quenching surface to generate the polyatomic form of the prescribed element.
  • the quenching surface includes a plurality of quenching surfaces, further including a plurality of flow channels having inputs and outputs. The flow channel inputs are disposed proximate an output of the plasma source.
  • the embodiment further includes a means for controlling a temperature of the quencher in a prescribed manner for producing a desired liquid-phase or gas-phase polyatomic form of the prescribed element.
  • the temperature control means includes a thermal channel in communication with the quencher suitable for passage of a prescribed coolant through the thermal channel.
  • the temperature control means further includes means for controlling a flow rate of coolant through the thermal channel.
  • the coolant includes liquid nitrogen, liquid helium, liquid oxygen, or other suitable coolant.
  • the prescribed element can include oxygen and the polyatomic form of the prescribed element includes ozone (O 3 ).
  • the embodiments of the present disclosure advantageously enable the generation of high concentration ozone (O 3 ), on the order of greater than fifty percent (>50%) and at a substantially limitless scalable production rate and volume.
  • the present embodiments enable the production of liquid O 3 at a substantially limitless scalable production rate and volume, for example, by a chemical plant. Having a scalable production rate and volume enables the usage of pure O 3 without the limitation of point-of-use O 3 generation. Accordingly, liquid O 3 can be transported, for example, in a suitable 161° K. refrigerated container or vessel.
  • a principal feature of the present embodiments is the surface O 3 generation through quenching of an oxygen (O 2 ) plasma.
  • Oxygen (O 2 ) gas of reasonable purity, or of a prescribed concentration level, is fed into a discharge vessel Of O 2 plasma.
  • the purity of the O 2 gas is on the order of between 99% to 99.999%. It is noted that other purities of O 2 gas can be used, however, the purity of the supply will influence the purity of generated ozone.
  • the O 2 plasma produces a substantially controllable ratio of O and O 2 mixture.
  • O 3 can be formed through a three-body collision in the gas-phase.
  • This three-body collision can be expressed as O+O 2 +h/ ⁇ O 3 , where h is the Planck's constant (6.63 ⁇ 10 ⁇ 34 joules-second, ⁇ is the wavelength of vibration, and h/ ⁇ represents a phonon (i.e., a quantum of vibrational energy).
  • O+O 2 +h/ ⁇ O 3 maintains the laws of conservation of momentum and the conservation of energy.
  • the third body h/ ⁇ is involved since the physical laws state that simultaneous conservation of both momentum and energy in a two-body only collision is impossible.
  • the probability of a three-body collision in the gas phase is extremely low.
  • the plasma is generally very hot.
  • the very hot plasma exponentially accelerates the decomposition of any O 3 , that may have formed. Accordingly, using O 2 plasma alone, the O 3 concentration resulting therefrom is extremely low.
  • the embodiments of the present disclosure employ a method of surface generation of O 3 .
  • the reaction of gas molecules O+O 2 ⁇ O 3 proceeds as a two-body process.
  • the two-body process has a much higher probability than the three-body collision in the gas-phase using the plasma alone.
  • the prescribed surface acts as the supplier of surface phonon.
  • the surface generation method of the present disclosure carries the two-body process one step further. That is, one body, namely O, collides with a “phonon and O 2 supply” surface to generate the desired output, O 3 .
  • the plasma is made to flow across a prescribed surface area that is maintained at a temperature lower than that of the plasma.
  • the prescribed surface area is of sufficient size and area to increase the probability of the plasma engaging the surface. Accordingly, the surface area is sufficient to guarantee that particles hit the surface (i.e., a large surface area with respect to the particle size).
  • the combination of surface area and surface temperature facilitate a process wherein O 2 from the plasma adsorbs (either physisorbs and/or chemisorbs) on the surface.
  • the adsorbed O 2 creates at least one thin layer, up to several or more molecular layers, of O 2 .
  • Adsorption is defined as the adhesion in an extremely thin layer of molecules (as of gases, solutes, or liquids) to the surface of solid bodies or liquids with which they are in contact. Accordingly, the adsorbed O 2 on the cold surface forms an O 2 and phonon supply surface.
  • the O from the plasma collides with the adsorbed O 2 , whereby O 3 is immediately formed, generally upon one collision.
  • the type of collision characterized by O from the plasma colliding with adsorbed O 2 can be viewed as a single-body colliding with a relatively large surface with limitless supply of phonon.
  • the probability of such collision is close to one (i.e. almost a certainty).
  • the temperature of the generation surface and that of the space near the generation surface is maintained sufficiently low (in comparison to the plasma temperature), such that the formed O 3 remains stable.
  • O 3 is formed.
  • additional adsorbed O 2 migrates and/or bubbles up from an inner layer 54 (or intermediate layer 56 ) to the outer layer 58 , such that the process of O 3 formation continues.
  • the layers (or layer) of adsorbed O 2 beneath the outer layer supply additional O 2 for subsequent O 3 generation.
  • the O 3 flows in a direction away from the plasma, either in gas-phase or liquid-phase.
  • an inert gas is added to the O 2 supply gas to assist in transporting formed O 3 away from and/or off of the O 3 generation surface.
  • the prescribed surface for use in O 3 generation is referred to herein as a quencher.
  • the quencher is characterized by a structure of cold surfaces relative to the plasma temperature.
  • the quencher is generally placed proximate an output boundary of the plasma. More particularly, the quencher is placed in the path of the plasma plume proximate the output boundary of the plasma.
  • the concentration ratio of O and O 2 is controllable, for example, by the feed gas O 2 flow rate, ambient pressure, and power input to the plasma, etc.
  • the temperature of the quencher surface is also controllable.
  • the temperature can be controlled by one or more suitable means, such as, the type of coolant used and the coolant flow rate through coolant channels within the quencher.
  • the type of adsorption (whether physisorption or chemisorption) is controllable, for example, by the type of surface material and/or surface chemical of the quencher.
  • Plasma flow and the corresponding flow pattern for facilitating ozone generation are controllable, for example, by a combination of the shape of the quencher, the characteristic bends and shapes of the flow channels, and the quencher flow channel surface shape(s).
  • the overall shape of the quencher and the quencher's surface shape can be configured by varying or changing the physical design of the quencher as may be required for a particular implementation.
  • a prescribed range of the process window parameters can be assembled and/or established. That is, a parameter window of process and hardware can be established within which i) all O 2 from the plasma that enter into the space of the quencher are adsorbed on the quencher surface and ii) wherein there is a sufficient amount of O, the O interacting with surface O 2 , such that substantially all the O and surface O 2 in the quencher are consumed, becoming O 3 .
  • the quencher surfaces are cold relative to the plasma temperature and therefore species inside the quencher space, such as gas-phase O, O 2 , and O 3 , are significantly colder than that in the plasma by an approximate order of magnitude lower.
  • the temperature of the gas-phase plasma is approximately 800° K.
  • the temperature of the quencher surface is approximately 100° K, and the temperature within the quencher space is approximately 200° K.
  • FIG. 2 illustrates another embodiment 100 of the method and apparatus of the present disclosure.
  • a plasma source 14 is mounted on a chamber 12 , the chamber for housing the quencher 20 and the resulting O 3 .
  • the plasma source 14 includes a plasma tube 64 .
  • Plasma source 14 receives a supply of oxygen gas at inlet 66 .
  • Electrical power is supplied at 68 .
  • Flow direction is indicated by arrow 70 .
  • the plasma source 14 can include any type plasma heated by a suitable method, such as inductive heating, capacitive heating, DC heating or wave heating (e.g., ECR, Helicon, etc.).
  • the quencher 20 is generally positioned proximate the output end of the plasma source. In one embodiment, the quencher 20 substantially occupies an entire area of the plasma output boundary for the purpose of achieving a higher efficiency.
  • the quencher 20 provides a large surface area (relative to the size of a particle), over which the species from the plasma (e.g., O, O 2 ) can flow across (or flow-by).
  • the geometry of the quencher's flow-path (i.e., its surface 52 ) and the type of the flow condition are selected in a prescribed manner to allow sufficient interaction between the flow species (e.g., O, O 2 , etc.) and the quencher's surfaces.
  • the quencher's flow path and flow condition facilitate adsorption of O 2 on the cold quencher surfaces and collision of O with the adsorbed O 2 , thereby leading to the surface generation of O 3 .
  • a suitable process control such as provided via controller 30 of FIG. 1, adjusts the quencher surface temperature as required for a particular implementation.
  • the general methodology of surface O 3 generation from an O 2 plasma is not limited to physisorption.
  • the flow-by O 2 or O can be placed on the surface through chemisorption, provided that an appropriate surface material is used.
  • the main point is that the surface can always act as the source of phonon to supply the necessary momentum for the reaction of O+O 2 ⁇ O 3 .
  • the particular reaction is not limited to the above reaction alone. There are other potential reaction channels through which O 3 can be generated on the quencher surface.
  • the boiling point for O 3 is approximately 161° K
  • the boiling point for O 2 is 90° K
  • the boiling point for N 2 is 77° K.
  • the quencher surface does not need to be as cold as the liquid-point at which the generated O 3 liquefies on the quencher surface under the chamber's particular pressure/temperature conditions.
  • the method of surface O 3 generation is satisfied.
  • the newly generated O 3 can be physisorbed on the quencher surface.
  • the physisorbed O 3 subsequently migrates down-stream away from the plasma and into the chamber for collection in a suitable collection vessel 72 and/or routing via suitable piping 74 , as appropriate.
  • the newly generated O 3 may have gained enough thermal energy from the flow-by species that the newly generated O 3 itself is desorbed from the quencher surface and transported down-stream into the chamber for collection and/or routing, as appropriate.
  • the coldness of the quencher surface cools down the gas-phase temperature, reducing and/or totally eliminating the probability of the decomposition of the generated/transported O 3 .
  • generating pure O 3 is accomplished with the quencher surface at a temperature satisfying the liquid-point of the generated O 3 (i.e., lower than the previous example).
  • the quencher surface temperature can be selected such that, under the chamber's pressure and temperature conditions, the flow-by O 2 physisorb on the quencher surface (but the surface temperature need not be so low as to have the adsorbed O 2 accumulate into liquid O 2 ) for the surface O 3 generation process. This is followed by the liquefaction of the generated O 3 on the quencher surface.
  • the quencher surface's liquid O 3 poses a vapor pressure that contributes to the output of the pure O 3 .
  • the plasma and the flow parameters can be adjusted as needed so that the substantial majority or entire flow-by O 2 are consumed for the production of high concentration or pure O 3 gas.
  • a suitable collection vessel provides for storage of the liquefied O 3 .
  • storage can be provided using any suitable liquid storage container known in the art.
  • FIG. 3 illustrates another embodiment 110 of the method and apparatus for generation of O 3 according to the present disclosure.
  • the plasma source 14 includes an inductive plasma.
  • the heated plasma volume is approximately 1.25′′ diameter X 3.5′′ long.
  • the pure O 2 feed rate is typically centered at approximately one to two standard liters per minute (1-2 slm).
  • the chamber 12 includes a stainless steel chamber such as that used within a typical laboratory environment.
  • the chamber includes a volume on the order of approximately 16′′ diameter X 23′′ long.
  • FIG. 4 illustrates a cross-section view of the exemplary quencher of FIG. 3 in greater detail.
  • the quencher is characterized by a “flow channels” design.
  • the flow channels 24 portion of the quencher assembly includes copper (Cu), for thermal considerations, with nickel (Ni) plating, for chemical protection.
  • FIGS. 5A and 5B show a top view and a cross sectional view of one of the Cu/Ni members or pieces of the quencher 20 , particularly illustrating the flow channels 24 in greater detail.
  • the quencher includes three Cu/Ni members or pieces that are silver-soldered together. Note that while this embodiment illustrates straight flow channels 24 , it should be noted that the flow channels could also include prescribed bends and/or shapes to further increase an interaction between the flow species and the quencher's surfaces, as may be needed for a particular design implementation.
  • the quencher assembly is mounted proximate the output end of the plasma source using suitable fasteners 80 .
  • suitable fasteners 80 For example, thermal isolators or ceramic posts may be used.
  • An input end 26 of the quencher 20 i.e., a top surface thereof
  • the input end 26 of the quencher is disposed approximately 3 mm from an end of the plasma tube (or plasma body) of the plasma source 14 .
  • Suitable thermal insulation is provided between the quencher and the chamber wall area, for example, via an ambient vacuum gap.
  • the system 110 is first drawn into a vacuum of approximately 5 mtorr (5 ⁇ 10 3 torr). Subsequent to achieving an initial vacuum, liquid nitrogen (LN 2 ) cooling is introduced. That is, LN 2 circulates through cooling channels 42 at a prescribed flow rate to cool the quencher 20 to a temperature of approximately 80° K, wherein the surface of the quencher being approximately 110° K. This step is followed by the introduction of flow of O 2 and ignition of the plasma. In response to ignition of the plasma, the process of surface generation of O 3 begins.
  • the R.F. power for the plasma source is on the order of 1200 W, and the pressure in the plasma region of the plasma source is approximately on the order of 2 to 3 torr.
  • the desorbed O 3 accumulates in and/or fills a down-stream area of the chamber.
  • the O 3 in the chamber can then be drawn out by the vacuum pump.
  • the O 3 can be stored in a suitable container, routed, and/or delivered to a prescribed oxidation application.
  • the examples presented herein are illustrative only and not intended to restrict the present embodiments.
  • the present embodiments include a methodology for manufacture of pure O 3 , high concentration O 3 , and liquid O 3 .
  • Other suitable apparatus can be assembled for carrying out the methodology of surface O 3 generation through the quenching of O 2 plasma.
  • the initial adsorption of the flow-by species can be accomplished through either physisorption (in this case, the physisorption of O 2 on a cold surface), or chemisorption by a surface of the adequate material (in this case, the chemisorption of O or O 2 ).
  • the surface uptake of flow-by species could be a combination of physisorption and chemisorption.
  • Apparatus or hardware for collection of liquid O 3 includes any suitable existing technology, which can be applied for use in the collection and storage of liquid O 3 .
  • the liquid O 3 on the surfaces of the quencher assembly is allowed to vaporize and expand.
  • the vaporized O 3 is then pumped out for storage and/or delivery to the particular oxidation application.
  • the present embodiments include a method and apparatus for producing pure O 3
  • the method and apparatus for producing pure O 3 further include applications requiring high concentration O 3 , pure O 3 , and liquid O 3 .
  • the present embodiments can be applied for sterilization, cleaning, deodorizing and general oxidation.
  • Liquid O 3 can also be stored and transported to a use location, other than the O 3 production location, to be dispensed for use in similar applications.
  • liquid O 3 can be used as an oxidizer of the rocket fuel in a rocket, thereby significantly reducing the volume and mass of the rocket at launch.
  • the present embodiments further include a system 120 for processing media 121 with ozone (O 3 ).
  • the media processing system 120 includes at least one processing vessel 122 ; suitable means 124 for disposing media to be processed into the at least one processing vessel; and means 126 for removing the processed media from said at least one processing vessel.
  • the media processing system includes means 128 for supplying ozone to the at least one processing vessel 122 to facilitate a processing of the media 121 by the ozone.
  • the ozone supplying means 128 is similar to that discussed herein with respect to FIGS. 1 - 3 .
  • the ozone supplying means includes a chamber, a plasma source coupled to the chamber, and a quencher disposed with the chamber proximate an output of the plasma source.
  • the plasma source produces an oxygen plasma from a supply of oxygen, the plasma including at least a mixture of O and O 2 species.
  • the quencher facilitates ozone generation from the mixture of O and O 2 species.
  • the processing system may also include a means 130 for destroying residual ozone subsequent to a processing of the media.
  • the residual ozone destructor 130 includes any suitable means known in the art for reducing the level of residual ozone to a prescribed safe level.
  • the residual ozone destructor 130 is used in conjunction with removal of the media from the processing chamber, further in preparation for discharge, for example, into atmosphere.
  • the present embodiments further include a method for processing media with ozone (O 3 ).
  • the method includes providing at least one processing vessel, disposing the media to be processed into the at least one processing vessel, supplying ozone to the at least one processing vessel to facilitate a processing of the media by the ozone, and removing the processed media from the at least one processing vessel subsequent to processing of the media by the ozone.
  • the method includes destroying residual ozone subsequent to ozone processing of the media.
  • a prescribed ozone generator supplies the ozone.
  • the ozone generator includes a generator as discussed herein with respect to FIGS. 1 - 3 .
  • the ozone generator includes a chamber, a plasma source coupled to the chamber for producing oxygen plasma from a supply of oxygen, and a quencher disposed within the chamber proximate an output of the plasma source.
  • the plasma includes at least a mixture of O and O 2 species.
  • the quencher facilitates ozone generation from the mixture of O and O 2 species.
  • the at least one processing vessel 122 of the media processing system and method 120 includes a processing chamber.
  • the processing chamber is characterized by an input and an output.
  • the means 124 for disposing media into the processing chamber couples to the input of the processing chamber.
  • the means 126 for removing the processed media from the processing chamber couples to the output of the processing chamber.
  • the processing chamber input and output represent a single portal.
  • the media processing system and method 120 are utilized in the manufacture of semiconductor devices.
  • the at least one processing vessel 122 includes a semiconductor substrate processing chamber and the media includes a semiconductor substrate.
  • the media processing system and method 120 are utilized for bioremediation of a gas, liquid, or solid media.
  • the at least one processing vessel 122 includes a bioremediation processing chamber and the media includes one of the following selected from the group consisting of gaseous media, liquid media, and solid media.

Abstract

A method and apparatus for generating a polyatomic form of a prescribed element is disclosed. The apparatus includes a chamber and a plasma source. The plasma source is coupled to the chamber for producing plasma of the prescribed element from a supply of the element in a gaseous state. The plasma includes at least a mixture of single atomic and double atomic species of the prescribed element. Lastly, a quencher is disposed within the chamber proximate an output of the plasma source for facilitating generation of the polyatomic form of the prescribed element from the mixture of single atomic and double atomic species of the prescribed element. In one embodiment, the element is oxygen and the polyatomic form is ozone.

Description

  • This application claims the benefits of the earlier filed provisional application Ser. No. 60/165,380 filed Nov. 12, 1999.[0001]
  • BACKGROUND
  • 1. Field of the Invention [0002]
  • The present invention relates generally to a methodology of generating ozone, and more particularly, to a method and apparatus for efficient surface generation of high concentration ozone and liquid ozone. [0003]
  • 2. Discussion of the Related Art [0004]
  • Prior to the embodiments of the present disclosure, generation of ozone (O[0005] 3) with high concentration (e.g., on the order of greater than twenty-five percent (25%)) and high rate of pure O3 generation have not been possible. A majority of the known state-of-the-art O3 generation is accomplished through corona discharge, which has a yield on the order of around ten to fifteen percent (10-15%) maximum and at a low generation rate. Usage of O3 has typically been limited to a low concentration (e.g., less than fifteen percent (<15%) and the generating of O3 constrained to being generated at the point-of-use.
  • Another method of ozone generation is UV ozone generation, which has an even lower concentration yield as compared to electric discharge ozone generation. A third and less popular method is electrolytic ozone generation. With electrolytic ozone generation, aqueous solutions of sulfuric or perchloric acid are electrolyzed with extremely high anodic current densities. In the later instance, oxygen (O[0006] 2) and, in the case of sulfuric acid solutions, peroxydisulfuric acid, H2S2O8, are by-products.
  • Accordingly, a method and apparatus for the generation of high concentration O[0007] 3 at the point-of-use (or at other than the point-of-use), and at a substantially limitless scalable production rate and volume are desired.
  • SUMMARY
  • According to one embodiment, an apparatus for generating ozone (O[0008] 3) includes a chamber and a plasma source. The plasma source couples to the chamber and produces oxygen plasma from a supply of oxygen. The plasma includes at least a mixture of O and O2 species. Lastly, a quencher is disposed within the chamber proximate an output of the plasma source for facilitating ozone generation from the mixture of O and O2 species.
  • A technical advantage provided by the embodiments of the present disclosure is the generation of high concentration O[0009] 3 at the point-of-use or location other than the point-of-use. In addition, the present embodiments provide the ability for achieving a substantially limitless scalable production rate and volume of high concentration O3.
  • BRIEF DESCRIPTION OF THE DRAWING
  • FIG. 1 illustrates a schematic view of an apparatus for surface generation of ozone according to an embodiment of the present disclosure; [0010]
  • FIG. 2 illustrates a schematic view of an apparatus for surface generation of ozone according to another embodiment of the present disclosure; [0011]
  • FIG. 3 illustrates a schematic view of an apparatus for surface generation of ozone according to another embodiment; [0012]
  • FIG. 4 illustrates a cross sectional view of a quencher of FIG. 3 in greater detail; [0013]
  • FIGS. 5A and 5B illustrate a top view and a cross section view of a portion of the quencher of FIG. 4; and [0014]
  • FIG. 6 illustrates a block diagram view of a system apparatus for processing media utilizing the method and apparatus for surface generation of ozone of the present disclosure.[0015]
  • DETAILED DESCRIPTION
  • With reference now to FIG. 1, an [0016] apparatus 10 for generating ozone (O3) includes a chamber 12, such as a vacuum chamber or other suitable chamber. A plasma source 14 couples to the chamber 12 for producing oxygen plasma 16 from a supply of oxygen 18. The plasma 16 includes at least a mixture of O and O2 species. A quencher 20 is disposed within the chamber 12 proximate an output of the plasma source 14 for facilitating ozone generation from the mixture of O and O2 species. The plasma source 14 includes an R.F. plasma source, a microwave source, or other suitable plasma sources. Electrical power is supplied to plasma source 14 as indicated by reference numeral 22.
  • The [0017] quencher 20 includes a quenching surface located down-stream of the plasma source within a prescribed region 17 of the oxygen plasma 16, such as in the plasma plume. The oxygen plasma flows across the quenching surface to generate ozone. In one embodiment, the quenching surface includes a plurality of quenching surfaces. Still further, the plurality of quenching surfaces include a plurality of flow channels 24 having inputs 26 and outputs 28, the inputs 26 being disposed proximate the output of the plasma source 14.
  • [0018] System apparatus 10 further includes a controller 30. Controller 30 includes any suitable programmable controller or computer for use in controlling various process parameters of the present method and apparatus. Process parameters are selected according to a prescribed process parameter window for a given ozone generation application (or for generation of a poly-atomic molecular form of a prescribed element). Controller 30 is programmed for performing desired functions as discussed herein. Programming may be accomplished using techniques well known in the art, thus not discussed further herein.
  • [0019] Controller 30 provides appropriate control signals for supply gas control 32, temperature control 34, plasma control 36, and vacuum pump control 38. Vacuum pump 40 provides a desired vacuum within chamber 12, as may be required for a given application. Controller 30 provides additional control signals, as may be needed, for control of additional parameters of a prescribed process window.
  • The [0020] apparatus 10 for generating ozone further includes means for controlling a temperature of the quencher in a prescribed manner for producing a desired form of liquid-phase or gas-phase ozone. Temperature control includes providing a thermal channel 42 in communication with the quencher 20 suitable for passage of a prescribed coolant through the thermal channel. The temperature control further includes controlling a flow rate of coolant through the thermal channel, such as, with a controllable flow valve or regulator (not shown). Controller 30 provides a temperature control signal 34, which may be used for controlling the flow valve or regulator, as appropriate. The coolant may include liquid nitrogen, liquid helium, liquid oxygen, or other suitable coolant.
  • As shown in FIG. 1, an enlarged [0021] view 50 of a portion of a flow channel 24 is shown. The enlarged view 50 illustrates several layers of adsorbed O2 on the quencher surface 52 of a flow channel 24. The layers of adsorbed O2 are characterized by an inner layer 54, intermediate layer (or layers) 56, and an outer layer 58, as discussed further herein below. Briefly, O from the mixture of O2 and O collide with the O2 from an outer layer 58 to produce O3. Depending upon the process parameters, O3 in the liquid phase 60 migrates to the quencher surface 52 (or O3 in the gas phase 62 flows within channel 24) to the output 28 of the respective flow channel 24.
  • With respect to a method for generating ozone (O[0022] 3), the method includes providing a chamber, such as a vacuum chamber or other suitable chamber. The method further includes providing a plasma source coupled to the chamber for producing oxygen plasma from a supply of oxygen. The plasma includes at least a mixture of O and O2 species. Lastly, a quencher is disposed within the chamber proximate an output of the plasma source for facilitating ozone generation from the mixture of O and O2 species. The plasma source includes an R.F. plasma source, a microwave source, or other suitable source.
  • Providing the quencher includes providing a quenching surface located down-stream of the plasma source within a prescribed region of the oxygen plasma, wherein the oxygen plasma flows across the quenching surface to generate ozone. In one embodiment, the quenching surface includes a plurality of quenching surfaces. The plurality of quenching surfaces include a plurality of flow channels having inputs and outputs, the inputs disposed proximate the output of the plasma source. [0023]
  • The method further includes controlling a temperature of the quencher in a prescribed manner for producing a desired form of liquid-phase or gas-phase ozone. Controlling the temperature of the quencher includes providing a thermal channel in communication with the quencher suitable for passage of a prescribed coolant through the thermal channel. Controlling the temperature further includes controlling a flow rate of coolant through the thermal channel. In one embodiment, the coolant includes liquid nitrogen, liquid helium, liquid oxygen, or other suitable coolant. [0024]
  • According to another embodiment, a method of generating ozone (O[0025] 3) includes supplying oxygen to a plasma source; igniting and producing an oxygen plasma with the plasma source, and directing the oxygen plasma for movement over a quenching surface of a quencher. The oxygen plasma contains a mixture of O and O2. The quenching surface is positioned down-stream of the plasma source within a prescribed region of the oxygen plasma. The oxygen plasma flows across the quenching surface to facilitate ozone generation from the mixture of O and O2. The quenching surface includes a plurality of flow channels disposed within the quencher, the flow channels having inputs and outputs. The flow channel inputs are arranged proximate an output of the plasma source.
  • The method further includes controlling a temperature of the quenching surface in a prescribed manner for producing a desired form of liquid-phase or gas-phase ozone. In addition, the temperature of the quenching surface may also be regulated. Regulating the temperature includes controlling the flow rate of a coolant flowing through a cooling channel disposed in the quencher. The coolant may include liquid nitrogen, liquid helium, liquid oxygen, or other suitable coolant. [0026]
  • The present embodiments further include an apparatus for generating a polyatomic form of a prescribed element. The apparatus includes a chamber, a plasma source coupled to the chamber, and a quencher. The plasma source produces plasma of the prescribed element from a supply of the element in a gaseous state. Accordingly, the plasma includes at least a mixture of single atomic, double atomic and polyatomic species of the prescribed element. The quencher is disposed within the chamber proximate an output of the plasma source. [0027]
  • The quencher facilitates generation of the polyatomic form of the prescribed element from the mixture of single atomic, double atomic and polyatomic species of the prescribed element. Similar to the other embodiments the plasma source includes an R.F. plasma source, a microwave source, or other suitable plasma source. The quencher includes a quenching surface located down-stream of the plasma source within a prescribed region of the plasma. The plasma flows across the quenching surface to generate the polyatomic form of the prescribed element. The quenching surface includes a plurality of quenching surfaces, further including a plurality of flow channels having inputs and outputs. The flow channel inputs are disposed proximate an output of the plasma source. [0028]
  • The embodiment further includes a means for controlling a temperature of the quencher in a prescribed manner for producing a desired liquid-phase or gas-phase polyatomic form of the prescribed element. The temperature control means includes a thermal channel in communication with the quencher suitable for passage of a prescribed coolant through the thermal channel. The temperature control means further includes means for controlling a flow rate of coolant through the thermal channel. The coolant includes liquid nitrogen, liquid helium, liquid oxygen, or other suitable coolant. The prescribed element can include oxygen and the polyatomic form of the prescribed element includes ozone (O[0029] 3).
  • The embodiments of the present disclosure advantageously enable the generation of high concentration ozone (O[0030] 3), on the order of greater than fifty percent (>50%) and at a substantially limitless scalable production rate and volume. The present embodiments enable the production of liquid O3 at a substantially limitless scalable production rate and volume, for example, by a chemical plant. Having a scalable production rate and volume enables the usage of pure O3 without the limitation of point-of-use O3 generation. Accordingly, liquid O3 can be transported, for example, in a suitable 161° K. refrigerated container or vessel.
  • A principal feature of the present embodiments is the surface O[0031] 3generation through quenching of an oxygen (O2) plasma. Oxygen (O2) gas of reasonable purity, or of a prescribed concentration level, is fed into a discharge vessel Of O2 plasma. In one embodiment, the purity of the O2 gas is on the order of between 99% to 99.999%. It is noted that other purities of O2 gas can be used, however, the purity of the supply will influence the purity of generated ozone.
  • The O[0032] 2 plasma produces a substantially controllable ratio of O and O2 mixture. With the oxygen plasma alone, O3 can be formed through a three-body collision in the gas-phase. This three-body collision can be expressed as O+O2+h/λ→O3, where h is the Planck's constant (6.63×10−34joules-second, λ is the wavelength of vibration, and h/λ represents a phonon (i.e., a quantum of vibrational energy). The expression O+O2+h/λ→O3 maintains the laws of conservation of momentum and the conservation of energy. The third body h/λ is involved since the physical laws state that simultaneous conservation of both momentum and energy in a two-body only collision is impossible.
  • The probability of a three-body collision in the gas phase, however, is extremely low. In addition, the plasma is generally very hot. The very hot plasma exponentially accelerates the decomposition of any O[0033] 3, that may have formed. Accordingly, using O2 plasma alone, the O3 concentration resulting therefrom is extremely low.
  • The embodiments of the present disclosure employ a method of surface generation of O[0034] 3. On a prescribed surface, the reaction of gas molecules O+O2→O3 proceeds as a two-body process. The two-body process has a much higher probability than the three-body collision in the gas-phase using the plasma alone. The prescribed surface acts as the supplier of surface phonon.
  • The probability of two bodies of certain momentum colliding with each other directly on a surface, where the surface acts as a limitless supplier of phonon, is higher than that of three bodies colliding in space. However, the two-body process alone is not extremely efficient in generating high concentration O[0035] 3. Accordingly, the surface generation method of the present disclosure carries the two-body process one step further. That is, one body, namely O, collides with a “phonon and O2 supply” surface to generate the desired output, O3.
  • To carry out the surface generation method of the present disclosure, the plasma is made to flow across a prescribed surface area that is maintained at a temperature lower than that of the plasma. The prescribed surface area is of sufficient size and area to increase the probability of the plasma engaging the surface. Accordingly, the surface area is sufficient to guarantee that particles hit the surface (i.e., a large surface area with respect to the particle size). [0036]
  • The combination of surface area and surface temperature facilitate a process wherein O[0037] 2 from the plasma adsorbs (either physisorbs and/or chemisorbs) on the surface. The adsorbed O2 creates at least one thin layer, up to several or more molecular layers, of O2. Adsorption is defined as the adhesion in an extremely thin layer of molecules (as of gases, solutes, or liquids) to the surface of solid bodies or liquids with which they are in contact. Accordingly, the adsorbed O2 on the cold surface forms an O2 and phonon supply surface. The O from the plasma collides with the adsorbed O2, whereby O3 is immediately formed, generally upon one collision.
  • The type of collision characterized by O from the plasma colliding with adsorbed O[0038] 2 can be viewed as a single-body colliding with a relatively large surface with limitless supply of phonon. The probability of such collision is close to one (i.e. almost a certainty). The temperature of the generation surface and that of the space near the generation surface is maintained sufficiently low (in comparison to the plasma temperature), such that the formed O3 remains stable.
  • Referring again to FIG. 1, as O collides with the O[0039] 2 on an outer layer 58 of the adsorbed O2, O3 is formed. Upon the formation of O3, additional adsorbed O2 migrates and/or bubbles up from an inner layer 54 (or intermediate layer 56) to the outer layer 58, such that the process of O3 formation continues. In other words, the layers (or layer) of adsorbed O2 beneath the outer layer supply additional O2 for subsequent O3 generation. In addition, upon generation, the O3 flows in a direction away from the plasma, either in gas-phase or liquid-phase. In an alternate embodiment, an inert gas is added to the O2 supply gas to assist in transporting formed O3 away from and/or off of the O3 generation surface.
  • The prescribed surface for use in O[0040] 3 generation is referred to herein as a quencher. The quencher is characterized by a structure of cold surfaces relative to the plasma temperature. The quencher is generally placed proximate an output boundary of the plasma. More particularly, the quencher is placed in the path of the plasma plume proximate the output boundary of the plasma.
  • The concentration ratio of O and O[0041] 2 is controllable, for example, by the feed gas O2 flow rate, ambient pressure, and power input to the plasma, etc. The temperature of the quencher surface is also controllable. For example, the temperature can be controlled by one or more suitable means, such as, the type of coolant used and the coolant flow rate through coolant channels within the quencher. The type of adsorption (whether physisorption or chemisorption) is controllable, for example, by the type of surface material and/or surface chemical of the quencher. Plasma flow and the corresponding flow pattern for facilitating ozone generation are controllable, for example, by a combination of the shape of the quencher, the characteristic bends and shapes of the flow channels, and the quencher flow channel surface shape(s). The overall shape of the quencher and the quencher's surface shape can be configured by varying or changing the physical design of the quencher as may be required for a particular implementation.
  • To obtain a maximum concentration of generated O[0042] 3 (on the order of approximately 100%), a prescribed range of the process window parameters can be assembled and/or established. That is, a parameter window of process and hardware can be established within which i) all O2 from the plasma that enter into the space of the quencher are adsorbed on the quencher surface and ii) wherein there is a sufficient amount of O, the O interacting with surface O2, such that substantially all the O and surface O2 in the quencher are consumed, becoming O3. In addition, as discussed herein, the quencher surfaces are cold relative to the plasma temperature and therefore species inside the quencher space, such as gas-phase O, O2, and O3, are significantly colder than that in the plasma by an approximate order of magnitude lower.
  • For example, in one embodiment, the temperature of the gas-phase plasma is approximately 800° K. The temperature of the quencher surface is approximately 100° K, and the temperature within the quencher space is approximately 200° K. [0043]
  • As mentioned herein above, gas-phase three-body generation of stable O[0044] 3 is still possible, although low in probability. A majority of O3 is generated on the quencher surface. In addition to the above discussion, another important effect of the coldness of the quencher (including the surface and the space thereof) is to allow the existence of stable O3 after its generation without suffering O3 decomposition.
  • FIG. 2 illustrates another [0045] embodiment 100 of the method and apparatus of the present disclosure. A plasma source 14 is mounted on a chamber 12, the chamber for housing the quencher 20 and the resulting O3. The plasma source 14 includes a plasma tube 64. Plasma source 14 receives a supply of oxygen gas at inlet 66. Electrical power is supplied at 68. In this embodiment, it is desirable to avoid having plasma actively discharged into the space of the quencher 20 and in the region down-stream from the quencher, so as to eliminate unnecessary heating of the quencher by the plasma. However, this does not exclude having the plasma in the chamber that houses the quencher where, in a particular situation, extra heating of the quencher by the extra plasma is not a concern. Flow direction is indicated by arrow 70.
  • The [0046] plasma source 14 can include any type plasma heated by a suitable method, such as inductive heating, capacitive heating, DC heating or wave heating (e.g., ECR, Helicon, etc.). The quencher 20 is generally positioned proximate the output end of the plasma source. In one embodiment, the quencher 20 substantially occupies an entire area of the plasma output boundary for the purpose of achieving a higher efficiency.
  • The [0047] quencher 20 provides a large surface area (relative to the size of a particle), over which the species from the plasma (e.g., O, O2) can flow across (or flow-by). The geometry of the quencher's flow-path (i.e., its surface 52) and the type of the flow condition are selected in a prescribed manner to allow sufficient interaction between the flow species (e.g., O, O2, etc.) and the quencher's surfaces. The quencher's flow path and flow condition facilitate adsorption of O2 on the cold quencher surfaces and collision of O with the adsorbed O2, thereby leading to the surface generation of O3. A suitable process control, such as provided via controller 30 of FIG. 1, adjusts the quencher surface temperature as required for a particular implementation.
  • It should be noted that the general methodology of surface O[0048] 3 generation from an O2 plasma is not limited to physisorption. The flow-by O2 or O can be placed on the surface through chemisorption, provided that an appropriate surface material is used. The main point is that the surface can always act as the source of phonon to supply the necessary momentum for the reaction of O+O2→O3. However, note that the particular reaction is not limited to the above reaction alone. There are other potential reaction channels through which O3 can be generated on the quencher surface.
  • In connection with the present embodiments, the boiling point for O[0049] 3 is approximately 161° K, the boiling point for O2 is 90° K, and the boiling point for N2 is 77° K. In the case of generating high concentration or pure O3 (gas phase), the quencher surface does not need to be as cold as the liquid-point at which the generated O3 liquefies on the quencher surface under the chamber's particular pressure/temperature conditions. According to the present embodiments, as long as the flow-by O2 can sufficiently physisorb on the quencher surface for a given duration of time such that the flow-by O can interact with the adsorbed O2 for the generation of O3, the method of surface O3 generation is satisfied.
  • In one embodiment, the newly generated O[0050] 3 can be physisorbed on the quencher surface. The physisorbed O3 subsequently migrates down-stream away from the plasma and into the chamber for collection in a suitable collection vessel 72 and/or routing via suitable piping 74, as appropriate. In another embodiment, the newly generated O3 may have gained enough thermal energy from the flow-by species that the newly generated O3 itself is desorbed from the quencher surface and transported down-stream into the chamber for collection and/or routing, as appropriate. The coldness of the quencher surface cools down the gas-phase temperature, reducing and/or totally eliminating the probability of the decomposition of the generated/transported O3.
  • In yet another embodiment, using a prescribed process window of chamber pressure and temperature conditions, generating pure O[0051] 3 is accomplished with the quencher surface at a temperature satisfying the liquid-point of the generated O3 (i.e., lower than the previous example). For example, the quencher surface temperature can be selected such that, under the chamber's pressure and temperature conditions, the flow-by O2 physisorb on the quencher surface (but the surface temperature need not be so low as to have the adsorbed O2 accumulate into liquid O2) for the surface O3 generation process. This is followed by the liquefaction of the generated O3 on the quencher surface. Under the appropriate chamber pressure and temperature condition, the quencher surface's liquid O3 poses a vapor pressure that contributes to the output of the pure O3. In addition, the plasma and the flow parameters can be adjusted as needed so that the substantial majority or entire flow-by O2 are consumed for the production of high concentration or pure O3 gas.
  • In the embodiments for producing liquid O[0052] 3, a suitable collection vessel provides for storage of the liquefied O3. For example, storage can be provided using any suitable liquid storage container known in the art.
  • FIG. 3 illustrates another [0053] embodiment 110 of the method and apparatus for generation of O3 according to the present disclosure. The plasma source 14 includes an inductive plasma. In this embodiment, the heated plasma volume is approximately 1.25″ diameter X 3.5″ long. The pure O2 feed rate is typically centered at approximately one to two standard liters per minute (1-2 slm). The chamber 12 includes a stainless steel chamber such as that used within a typical laboratory environment. The chamber includes a volume on the order of approximately 16″ diameter X 23″ long.
  • FIG. 4 illustrates a cross-section view of the exemplary quencher of FIG. 3 in greater detail. According to one embodiment, the quencher is characterized by a “flow channels” design. The [0054] flow channels 24 portion of the quencher assembly includes copper (Cu), for thermal considerations, with nickel (Ni) plating, for chemical protection. FIGS. 5A and 5B show a top view and a cross sectional view of one of the Cu/Ni members or pieces of the quencher 20, particularly illustrating the flow channels 24 in greater detail. In one embodiment, the quencher includes three Cu/Ni members or pieces that are silver-soldered together. Note that while this embodiment illustrates straight flow channels 24, it should be noted that the flow channels could also include prescribed bends and/or shapes to further increase an interaction between the flow species and the quencher's surfaces, as may be needed for a particular design implementation.
  • Referring to FIGS. [0055] 3-5, the quencher assembly is mounted proximate the output end of the plasma source using suitable fasteners 80. For example, thermal isolators or ceramic posts may be used. An input end 26 of the quencher 20 (i.e., a top surface thereof) is proximate to and borders a plasma body of a plasma to be produced by the plasma source 14. In one embodiment, the input end 26 of the quencher is disposed approximately 3 mm from an end of the plasma tube (or plasma body) of the plasma source 14. Suitable thermal insulation is provided between the quencher and the chamber wall area, for example, via an ambient vacuum gap.
  • In operation, according to one embodiment, the [0056] system 110 is first drawn into a vacuum of approximately 5 mtorr (5×103 torr). Subsequent to achieving an initial vacuum, liquid nitrogen (LN2) cooling is introduced. That is, LN2 circulates through cooling channels 42 at a prescribed flow rate to cool the quencher 20 to a temperature of approximately 80° K, wherein the surface of the quencher being approximately 110° K. This step is followed by the introduction of flow of O2 and ignition of the plasma. In response to ignition of the plasma, the process of surface generation of O3 begins. In one embodiment, the R.F. power for the plasma source is on the order of 1200 W, and the pressure in the plasma region of the plasma source is approximately on the order of 2 to 3 torr.
  • Accumulation of liquid O[0057] 3 on the quencher surfaces starts to occur almost immediately following the ignition of the plasma. As liquid O3 accumulates thicker within the quencher, the liquid O3 surface is subject to boil (i.e., via vaporization into the chamber) due to both the thermal isolation by the liquid O3 itself from the quencher surface and the action of the flow-by species. At the entrance of the quencher assembly, the flow-by species are largely O/O2 mixture. Towards the end of the quencher assembly, the flow-by species becomes largely O3 (i.e., the desorbed O3 or vaporized O3). For example, with a proper adjustment of the initial O/O2 mixture from the plasma and the total flow rate, a substantially complete depletion of O2 can be accomplished at the exit of the quencher assembly. Accordingly, the desorbed O3 accumulates in and/or fills a down-stream area of the chamber. The O3 in the chamber can then be drawn out by the vacuum pump. In addition, the O3 can be stored in a suitable container, routed, and/or delivered to a prescribed oxidation application.
  • The examples presented herein are illustrative only and not intended to restrict the present embodiments. The present embodiments include a methodology for manufacture of pure O[0058] 3, high concentration O3, and liquid O3. Other suitable apparatus can be assembled for carrying out the methodology of surface O3 generation through the quenching of O2 plasma.
  • The initial adsorption of the flow-by species (O/O[0059] 2) can be accomplished through either physisorption (in this case, the physisorption of O2 on a cold surface), or chemisorption by a surface of the adequate material (in this case, the chemisorption of O or O2). Also, the surface uptake of flow-by species could be a combination of physisorption and chemisorption. For example, in the above discussed implementation of FIG. 4, it is possible, although believed low in occurrence, that some flow-by O gets weakly chemisorbed on the quencher surface and surface O3 is subsequently formed by a flow-by O2 or other flow-by single molecule oxygen (O). It is important to significantly lower the gas-phase species temperature as the species flow through the “surface apparatus,” to a point that is much lower than that of the plasma so that the probability of O3 decomposition is drastically reduced.
  • Apparatus or hardware for collection of liquid O[0060] 3 includes any suitable existing technology, which can be applied for use in the collection and storage of liquid O3. For gas O3, the liquid O3 on the surfaces of the quencher assembly is allowed to vaporize and expand. The vaporized O3 is then pumped out for storage and/or delivery to the particular oxidation application.
  • While the present embodiments include a method and apparatus for producing pure O[0061] 3, the method and apparatus for producing pure O3 further include applications requiring high concentration O3, pure O3, and liquid O3. As a point-of-use O3 source, the present embodiments can be applied for sterilization, cleaning, deodorizing and general oxidation. Liquid O3 can also be stored and transported to a use location, other than the O3 production location, to be dispensed for use in similar applications. For example, liquid O3 can be used as an oxidizer of the rocket fuel in a rocket, thereby significantly reducing the volume and mass of the rocket at launch.
  • Turning now to FIG. 6, the present embodiments further include a [0062] system 120 for processing media 121 with ozone (O3). The media processing system 120 includes at least one processing vessel 122; suitable means 124 for disposing media to be processed into the at least one processing vessel; and means 126 for removing the processed media from said at least one processing vessel.
  • In addition, the media processing system includes means [0063] 128 for supplying ozone to the at least one processing vessel 122 to facilitate a processing of the media 121 by the ozone. The ozone supplying means 128 is similar to that discussed herein with respect to FIGS. 1-3. The ozone supplying means includes a chamber, a plasma source coupled to the chamber, and a quencher disposed with the chamber proximate an output of the plasma source. The plasma source produces an oxygen plasma from a supply of oxygen, the plasma including at least a mixture of O and O2 species. The quencher facilitates ozone generation from the mixture of O and O2 species.
  • The processing system may also include a [0064] means 130 for destroying residual ozone subsequent to a processing of the media. The residual ozone destructor 130 includes any suitable means known in the art for reducing the level of residual ozone to a prescribed safe level. The residual ozone destructor 130 is used in conjunction with removal of the media from the processing chamber, further in preparation for discharge, for example, into atmosphere.
  • The present embodiments further include a method for processing media with ozone (O[0065] 3). The method includes providing at least one processing vessel, disposing the media to be processed into the at least one processing vessel, supplying ozone to the at least one processing vessel to facilitate a processing of the media by the ozone, and removing the processed media from the at least one processing vessel subsequent to processing of the media by the ozone. In addition, the method includes destroying residual ozone subsequent to ozone processing of the media.
  • For the method of processing media, a prescribed ozone generator supplies the ozone. The ozone generator includes a generator as discussed herein with respect to FIGS. [0066] 1-3. The ozone generator includes a chamber, a plasma source coupled to the chamber for producing oxygen plasma from a supply of oxygen, and a quencher disposed within the chamber proximate an output of the plasma source. The plasma includes at least a mixture of O and O2 species. The quencher facilitates ozone generation from the mixture of O and O2 species.
  • In one embodiment, the at least one [0067] processing vessel 122 of the media processing system and method 120 includes a processing chamber. The processing chamber is characterized by an input and an output. The means 124 for disposing media into the processing chamber couples to the input of the processing chamber. The means 126 for removing the processed media from the processing chamber couples to the output of the processing chamber. In one embodiment, the processing chamber input and output represent a single portal.
  • In another embodiment, the media processing system and [0068] method 120 are utilized in the manufacture of semiconductor devices. In this instance, the at least one processing vessel 122 includes a semiconductor substrate processing chamber and the media includes a semiconductor substrate.
  • In another embodiment, the media processing system and [0069] method 120 are utilized for bioremediation of a gas, liquid, or solid media. In this instance, the at least one processing vessel 122 includes a bioremediation processing chamber and the media includes one of the following selected from the group consisting of gaseous media, liquid media, and solid media.
  • While the invention has been particularly shown and described with reference to the preferred embodiment thereof, it will be understood by those skilled in the art that various changes in form and detail may be made therein without departing from the spirit and scope of the invention, as set forth in the following claims. [0070]

Claims (46)

What is claimed is:
1. An apparatus for generating ozone (O3) comprising:
a chamber;
a plasma source coupled to said chamber for producing an oxygen plasma from a supply of oxygen, the plasma including at least a mixture of O and O2 species; and
a quencher disposed within said chamber proximate an output of said plasma source for facilitating ozone generation from the mixture of O and O2 species.
2. The apparatus of claim 1, wherein said plasma source includes one of the following selected from the group consisting of an r.f. plasma source and a microwave source.
3. The apparatus of claim 1, wherein said quencher includes a quenching surface located down-stream of said plasma source within a prescribed region of the oxygen plasma, wherein the oxygen plasma flows across the quenching surface to generate ozone.
4. The apparatus of claim 3, further wherein the quenching surface includes a plurality of quenching surfaces.
5. The apparatus of claim 4, still further wherein the plurality of quenching surfaces include a plurality of flow channels having inputs and outputs, the inputs disposed proximate the output of said plasma source.
6. The apparatus of claim 1, further comprising:
means for controlling a temperature of said quencher in a prescribed manner for producing a desired form of liquid-phase or gas-phase ozone.
7. The apparatus of claim 6, wherein said temperature control means includes a thermal channel in communication with said quencher suitable for passage of a prescribed coolant through the thermal channel.
8. The apparatus of claim 7, wherein said temperature control means further includes means for controlling a flow rate of coolant through the thermal channel.
9. The apparatus of claim 7, wherein the coolant includes one of the following selected from the group consisting of liquid nitrogen, liquid helium, and liquid oxygen.
10. An apparatus for generating ozone (O3) comprising:
a chamber;
a plasma source coupled to said chamber for producing an oxygen plasma from a supply of oxygen, the plasma including at least a mixture of O and O2 species;
a quencher disposed within said chamber proximate an output of said plasma source for facilitating ozone generation from the mixture of O and O2 species, wherein said quencher includes a plurality of quenching surfaces located down-stream of said plasma source within a prescribed region of the oxygen plasma, the plurality of quenching surfaces including flow channels having inputs and outputs, the inputs disposed proximate the output of said plasma source, wherein the oxygen plasma flows across the quenching surfaces to generate ozone; and
means for controlling a temperature of said quencher in a prescribed manner for producing a desired form of liquid-phase or gas-phase ozone, said control means including at least one channel in thermal communication with said quencher suitable for passage of a prescribed coolant through the channel, said control means further including a controllable flow valve for controlling a flow rate of coolant through the channel.
11. A method for generating ozone (O3) comprising:
providing a chamber;
providing a plasma source coupled to the chamber for producing an oxygen plasma from a supply of oxygen, the plasma including at least a mixture of O and O2 species; and
disposing a quencher within the chamber proximate an output of the plasma source for facilitating ozone generation from the mixture of O and O2 species.
12. The method of claim 11, wherein providing the plasma source includes providing one of the following selected from the group consisting of an r.f. plasma source and a microwave source.
13. The method of claim 11, wherein providing the quencher includes providing a quenching surface located down-stream of the plasma source within a prescribed region of the oxygen plasma, wherein the oxygen plasma flows across the quenching surface to generate ozone.
14. The method of claim 13, wherein the quenching surface includes a plurality of quenching surfaces.
15. The method of claim 14, further wherein the plurality of quenching surfaces include a plurality of flow channels having inputs and outputs, the inputs disposed proximate the output of the plasma source.
16. The method of claim 11, further comprising:
controlling a temperature of the quencher in a prescribed manner for producing a desired form of liquid-phase or gas-phase ozone.
17. The method of claim 16, wherein controlling the temperature of the quencher includes providing a thermal channel in communication with the quencher suitable for passage of a prescribed coolant through the thermal channel.
18. The method of claim 17, wherein controlling the temperature further includes controlling a flow rate of coolant through the thermal channel.
19. The method of claim 17, wherein the coolant includes one of the following selected from the group consisting of liquid nitrogen, liquid helium, and liquid oxygen.
20. A method for generating ozone (O3) comprising:
providing a chamber;
providing a plasma source coupled to the chamber for producing an oxygen plasma from a supply of oxygen, the plasma including at least a mixture of O and O2 species;
disposing a quencher within the chamber proximate an output of the plasma source for facilitating ozone generation from the mixture of O and O2 species, wherein the quencher includes a plurality of quenching surfaces located down-stream of the plasma source within a prescribed region of the oxygen plasma, the plurality of quenching surfaces including flow channels having inputs and outputs, the inputs disposed proximate the output of the plasma source, wherein the oxygen plasma flows across the quenching surfaces to generate ozone; and
controlling a temperature of the quencher in a prescribed manner for producing a desired form of liquid-phase or gas-phase ozone, wherein controlling the temperature includes providing at least one channel in thermal communication with the quencher suitable for passage of a prescribed coolant through the channel and providing a controllable flow valve for controlling a flow rate of coolant through the channel.
21. A method of generating ozone (O3) comprising:
supplying oxygen to a plasma source;
igniting and producing an oxygen plasma with the plasma source, the oxygen plasma including a mixture of O and O2; and
directing the oxygen plasma for movement over a quenching surface of a quencher, the quenching surface located down-stream of the plasma source within a prescribed region of the oxygen plasma, wherein the oxygen plasma flows across the quenching surface to facilitate ozone generation from the mixture of O and O2.
22. The method of claim 21, further comprising:
controlling a temperature of the quenching surface in a prescribed manner for producing a desired form of liquid-phase or gas-phase ozone.
23. The method of claim 21, wherein the quenching surface includes a plurality of flow channels disposed within the quencher, the flow channels having inputs and outputs, the inputs arranged proximate an output of the plasma source.
24. The method of claim 23, further comprising:
regulating a temperature of the quenching surface.
25. The method of claim 24, wherein regulating the temperature includes controlling the flow rate of a coolant flowing through a cooling channel disposed in the quencher.
26. The method of claim 25, wherein the coolant includes one of the following selected from the group consisting of liquid nitrogen, liquid helium, and liquid oxygen.
27. An apparatus for generating a polyatomic form of a prescribed element comprising:
a chamber;
a plasma source coupled to said chamber for producing plasma of the prescribed element from a supply of the element in a gaseous state, the plasma including at least a mixture of single atomic and double atomic species of the prescribed element; and
a quencher disposed within said chamber proximate an output of said plasma source for facilitating generation of the polyatomic form of the prescribed element from the mixture of single atomic and double atomic species of the prescribed element.
28. The apparatus of claim 27, wherein said plasma source includes one of the following selected from the group consisting of an r.f. plasma source and a microwave source.
29. The apparatus of claim 27, wherein said quencher includes a quenching surface located down-stream of said plasma source within a prescribed region of the plasma, wherein the plasma flows across the quenching surface to generate the polyatomic form of the prescribed element.
30. The apparatus of claim 29, further wherein the quenching surface includes a plurality of quenching surfaces.
31. The apparatus of claim 30, still further wherein the plurality of quenching surfaces include a plurality of flow channels having inputs and outputs, the inputs disposed proximate the output of said plasma source.
32. The apparatus of claim 27, further comprising:
means for controlling a temperature of said quencher in a prescribed manner for producing a desired liquid-phase or gas-phase polyatomic form of the prescribed element.
33. The apparatus of claim 32, wherein said temperature control means includes a thermal channel in communication with said quencher suitable for passage of a prescribed coolant through the thermal channel.
34. The apparatus of claim 33, wherein said temperature control means further includes means for controlling a flow rate of coolant through the thermal channel.
35. The apparatus of claim 33, wherein the coolant includes one of the following selected from the group consisting of liquid nitrogen, liquid helium, and liquid oxygen.
36. The apparatus of claim 27, wherein the prescribed element includes oxygen and the polyatomic form of the prescribed element includes ozone (O3).
37. A system for processing media with ozone (O3) comprising:
at least one processing vessel;
means for disposing media to be processed into said at least one processing vessel;
means for supplying ozone to said at least one processing vessel to facilitate a processing of the media by the ozone, said ozone supplying means including a chamber, a plasma source coupled to the chamber for producing an oxygen plasma from a supply of oxygen, the plasma including at least a mixture of O and O2 species, and a quencher disposed within the chamber proximate an output of the plasma source for facilitating ozone generation from the mixture of O and O2 species; and
means for removing the processed media from said at least one processing vessel.
38. The system of claim 37, further comprising:
means for destroying residual ozone subsequent to a processing of the media.
39. The system of claim 37, wherein said at least one processing vessel includes a processing chamber, the processing chamber having an input and an output, wherein said means for disposing media into the processing chamber is coupled to the input of the processing chamber, and said means for removing the processed media from the processing chamber is coupled to the output of the processing chamber.
40. The system of claim 37, wherein said at least one processing vessel includes a semiconductor substrate processing chamber and the media includes a semiconductor substrate.
41. The system of claim 37, wherein said at least one processing vessel includes a bioremediation processing chamber and the media includes one of the following selected from the group consisting of gaseous media, liquid media, and solid media.
42. A method for processing media with ozone (O3) comprising:
providing at least one processing vessel;
disposing media to be processed into the at least one processing vessel;
supplying ozone to the at least one processing vessel to facilitate a processing of the media by the ozone, wherein supplying ozone is provided by an ozone generator including a chamber, a plasma source coupled to the chamber for producing an oxygen plasma from a supply of oxygen, the plasma including at least a mixture of 0 and O2 species, and a quencher disposed within the chamber proximate an output of the plasma source for facilitating ozone generation from the mixture of O and O2 species; and
removing the processed media from the at least one processing vessel subsequent to processing of the media by the ozone.
43. The method of claim 42, further comprising:
destroying residual ozone subsequent to ozone processing of the media.
44. The method of claim 42, wherein the at least one processing vessel includes a processing chamber, the processing chamber having an input and an output, wherein said disposing the media into the processing chamber is coupled through the input of the processing chamber and said removing the processed media from the processing chamber is coupled through the output of the processing chamber.
45. The method of claim 42, wherein the at least one processing vessel includes a semiconductor substrate processing chamber and the media includes a semiconductor substrate.
46. The method of claim 42, wherein the at least one processing vessel includes a bioremediation processing chamber and the media includes one of the following selected from the group consisting of a gaseous media and a porous solid media.
US10/034,084 1999-11-12 2001-12-28 Method and apparatus for efficient surface generation of pure O3 Abandoned US20020054839A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US10/034,084 US20020054839A1 (en) 1999-11-12 2001-12-28 Method and apparatus for efficient surface generation of pure O3

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US16538099P 1999-11-12 1999-11-12
US09/549,269 US6372097B1 (en) 1999-11-12 2000-04-14 Method and apparatus for efficient surface generation of pure O3
US10/034,084 US20020054839A1 (en) 1999-11-12 2001-12-28 Method and apparatus for efficient surface generation of pure O3

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US09/549,269 Continuation US6372097B1 (en) 1999-11-12 2000-04-14 Method and apparatus for efficient surface generation of pure O3

Publications (1)

Publication Number Publication Date
US20020054839A1 true US20020054839A1 (en) 2002-05-09

Family

ID=26861343

Family Applications (2)

Application Number Title Priority Date Filing Date
US09/549,269 Expired - Fee Related US6372097B1 (en) 1999-11-12 2000-04-14 Method and apparatus for efficient surface generation of pure O3
US10/034,084 Abandoned US20020054839A1 (en) 1999-11-12 2001-12-28 Method and apparatus for efficient surface generation of pure O3

Family Applications Before (1)

Application Number Title Priority Date Filing Date
US09/549,269 Expired - Fee Related US6372097B1 (en) 1999-11-12 2000-04-14 Method and apparatus for efficient surface generation of pure O3

Country Status (1)

Country Link
US (2) US6372097B1 (en)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5975090A (en) 1998-09-29 1999-11-02 Sharper Image Corporation Ion emitting grooming brush
US6544485B1 (en) 2001-01-29 2003-04-08 Sharper Image Corporation Electro-kinetic device with enhanced anti-microorganism capability
US6974560B2 (en) * 1998-11-05 2005-12-13 Sharper Image Corporation Electro-kinetic air transporter and conditioner device with enhanced anti-microorganism capability
US6958134B2 (en) 1998-11-05 2005-10-25 Sharper Image Corporation Electro-kinetic air transporter-conditioner devices with an upstream focus electrode
US6176977B1 (en) 1998-11-05 2001-01-23 Sharper Image Corporation Electro-kinetic air transporter-conditioner
US7695690B2 (en) * 1998-11-05 2010-04-13 Tessera, Inc. Air treatment apparatus having multiple downstream electrodes
US20030206837A1 (en) * 1998-11-05 2003-11-06 Taylor Charles E. Electro-kinetic air transporter and conditioner device with enhanced maintenance features and enhanced anti-microorganism capability
US6350417B1 (en) * 1998-11-05 2002-02-26 Sharper Image Corporation Electrode self-cleaning mechanism for electro-kinetic air transporter-conditioner devices
US6632407B1 (en) * 1998-11-05 2003-10-14 Sharper Image Corporation Personal electro-kinetic air transporter-conditioner
US20050210902A1 (en) 2004-02-18 2005-09-29 Sharper Image Corporation Electro-kinetic air transporter and/or conditioner devices with features for cleaning emitter electrodes
US6585935B1 (en) 1998-11-20 2003-07-01 Sharper Image Corporation Electro-kinetic ion emitting footwear sanitizer
US6727140B2 (en) * 2001-07-11 2004-04-27 Micron Technology, Inc. Capacitor with high dielectric constant materials and method of making
US6749667B2 (en) 2002-06-20 2004-06-15 Sharper Image Corporation Electrode self-cleaning mechanism for electro-kinetic air transporter-conditioner devices
US7056370B2 (en) * 2002-06-20 2006-06-06 Sharper Image Corporation Electrode self-cleaning mechanism for air conditioner devices
US20040136885A1 (en) * 2003-01-09 2004-07-15 Hogarth Derek J. Apparatus and method for generating ozone
US7029637B2 (en) * 2003-01-09 2006-04-18 H203, Inc. Apparatus for ozone production, employing line and grooved electrodes
US6984987B2 (en) * 2003-06-12 2006-01-10 Sharper Image Corporation Electro-kinetic air transporter and conditioner devices with enhanced arching detection and suppression features
GB0318017D0 (en) * 2003-08-01 2003-09-03 Shipley Co Llc Methods for recovering metals
US7906080B1 (en) 2003-09-05 2011-03-15 Sharper Image Acquisition Llc Air treatment apparatus having a liquid holder and a bipolar ionization device
US7724492B2 (en) 2003-09-05 2010-05-25 Tessera, Inc. Emitter electrode having a strip shape
US20050082160A1 (en) * 2003-10-15 2005-04-21 Sharper Image Corporation Electro-kinetic air transporter and conditioner devices with a mesh collector electrode
US7767169B2 (en) 2003-12-11 2010-08-03 Sharper Image Acquisition Llc Electro-kinetic air transporter-conditioner system and method to oxidize volatile organic compounds
US20050146712A1 (en) * 2003-12-24 2005-07-07 Lynx Photonics Networks Inc. Circuit, system and method for optical switch status monitoring
US20060016333A1 (en) 2004-07-23 2006-01-26 Sharper Image Corporation Air conditioner device with removable driver electrodes
US20060263281A1 (en) * 2005-05-20 2006-11-23 Dial Discoveries Llc Systems and methods for treatment of various environments by application of ozone and steam
US7833322B2 (en) 2006-02-28 2010-11-16 Sharper Image Acquisition Llc Air treatment apparatus having a voltage control device responsive to current sensing

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4095115A (en) * 1976-12-27 1978-06-13 Accelerators, Inc. Ozone generation apparatus and method
US4167466A (en) * 1976-12-27 1979-09-11 Accelerators, Inc. Ozone generation apparatus and method
US5332555A (en) * 1990-07-27 1994-07-26 Agency Of Industrial Science & Technology Ozone beam generation apparatus and method for generating an ozone beam
US5624734A (en) * 1996-02-21 1997-04-29 Rees; Darci L. Continuous process and apparatus for generation of ozone for industrial application with cryogenic refrigeration
US5756054A (en) * 1995-06-07 1998-05-26 Primex Technologies Inc. Ozone generator with enhanced output
US5785824A (en) * 1995-09-28 1998-07-28 Mitsubishi Denki Kabushiki Kaisha Method of and apparatus for producing ozone
US6193852B1 (en) * 1997-05-28 2001-02-27 The Boc Group, Inc. Ozone generator and method of producing ozone

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4095115A (en) * 1976-12-27 1978-06-13 Accelerators, Inc. Ozone generation apparatus and method
US4167466A (en) * 1976-12-27 1979-09-11 Accelerators, Inc. Ozone generation apparatus and method
US5332555A (en) * 1990-07-27 1994-07-26 Agency Of Industrial Science & Technology Ozone beam generation apparatus and method for generating an ozone beam
US5756054A (en) * 1995-06-07 1998-05-26 Primex Technologies Inc. Ozone generator with enhanced output
US5785824A (en) * 1995-09-28 1998-07-28 Mitsubishi Denki Kabushiki Kaisha Method of and apparatus for producing ozone
US5624734A (en) * 1996-02-21 1997-04-29 Rees; Darci L. Continuous process and apparatus for generation of ozone for industrial application with cryogenic refrigeration
US6193852B1 (en) * 1997-05-28 2001-02-27 The Boc Group, Inc. Ozone generator and method of producing ozone

Also Published As

Publication number Publication date
US6372097B1 (en) 2002-04-16

Similar Documents

Publication Publication Date Title
US6372097B1 (en) Method and apparatus for efficient surface generation of pure O3
USRE34806E (en) Magnetoplasmadynamic processor, applications thereof and methods
Fridman Plasma chemistry
US6656540B2 (en) Method for forming metallic film and apparatus for forming the same
Selwyn et al. Materials Processing Using an Atmospheric Pressure, RF‐Generated Plasma Source
US5632868A (en) Method and apparatus for generating ozone and methods of its use
WO2008004278A1 (en) Apparatus for concentrating/diluting specific gas and method of concentrating/diluting specific gas
US4682564A (en) Magnetoplasmadynamic processor, applications thereof and methods
WO2004042798A2 (en) Apparatus and method for treating objects with radicals generated from plasma
US5821548A (en) Beam source for production of radicals and metastables
US7446289B2 (en) Enhanced plasma filter
US3407281A (en) Plasma producing apparatus
Mori et al. Characterization of a capillary plasma reactor for carbon dioxide decomposition
Engeln et al. Plasma expansion: fundamentals and applications
CN1764738B (en) Apparatus and method for depositing large area coating on explanate surface
US6509067B2 (en) Method and apparatus for the deposition of metal nanoclusters and films on a substrate
Ichimura et al. Development of a continuous generation/supply system of highly concentrated ozone gas for low-temperature oxidation process
KR101163643B1 (en) Apparatus for generating plasma at atmosphericpressure
Schram et al. Plasma processing and chemistry
US5318684A (en) Systems for the decomposition of water
JP2001295046A (en) Vapor phase growth system of copper thin film
SELWYN et al. MATERIALS PROCESSING USING AN ATMOSPHERIC PRESSURE PLASMA JET
KR20080029346A (en) Vaporizer and method of vaporizing and cleaning method of vaporizer having high evaporating efficiency using plasma
JP2001139309A (en) Liquefied ozone generating device
JP5290841B2 (en) Metal film production apparatus and metal film production method

Legal Events

Date Code Title Description
STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION