Electrode cleaning in an electro-kinetic air mover

Information

  • Patent Grant
  • 8425658
  • Patent Number
    8,425,658
  • Date Filed
    Friday, May 20, 2011
    13 years ago
  • Date Issued
    Tuesday, April 23, 2013
    11 years ago
Abstract
An electro-kinetic or electro-static apparatus for moving fluid includes an enlogated electrode energizable with respect to at least one other electrode to generate ions and thereby motivate fluid flow there between. A cleaning device is positioned to frictionally engage at least two opposing surfaces of the elongated electrode. The cleaning device is movable along a length of the elongated electrode to thereby remove detrimental material from the at least two opposing surfaces of the elongated electrode. The cleaning device can be substantially off-center relative to the elongated electrode to frictionally bind upon the elongated electrode during movement of the cleaning device.
Description
BACKGROUND

1. Field of the Invention


The present invention relates generally to devices that produce an electro-kinetic flow of air from which particulate matter is substantially removed.


2. Description of the Related Art


The use of an electric motor to rotate a fan blade to create an airflow has long been known in the art. Unfortunately, such fans produce substantial noise, and can present a hazard to children who may be tempted to poke a finger or a pencil into the moving fan blade. Although such fans can produce substantial airflow (e.g., 1,000 ft3/minute or more), substantial electrical power is required to operate the motor, and essentially no conditioning of the flowing air occurs.


It is known to provide such fans with a HEPA-compliant filter element to remove particulate matter larger than perhaps 0.3 μm. Unfortunately, the resistance to airflow presented by the filter element may require doubling the electric motor size to maintain a desired level of airflow. Further, HEPA-compliant filter elements are expensive, and can represent a substantial portion of the sale price of a HEPA-compliant filter-fan unit. While such filter-fan units can condition the air by removing large particles, particulate matter small enough to pass through the filter element is not removed, including bacteria, for example.


It is also known in the art to produce an airflow using electro-kinetic techniques, by which electrical power is converted into a flow of air without mechanically moving components. One such system is described in U.S. Pat. No. 4,789,801 to Lee (1988), depicted herein in simplified form as FIGS. 1A and 1B and which patent is incorporated herein by reference. System 10 includes an array of first (“emitter”) electrodes or conductive surfaces 20 that are spaced-apart symmetrically from an array of second (“collector”) electrodes or conductive surfaces 30. The positive terminal of a generator such as, for example, pulse generator 40 that outputs a train of high voltage pulses (e.g., 0 to perhaps +5 KV) is coupled to the first array, and the negative pulse generator terminal is coupled to the second array in this example. It is to be understood that the arrays depicted include multiple electrodes, but that an array can include or be replaced by a single electrode.


The high voltage pulses ionize the air between the arrays, and create an airflow 50 from the first array toward the second array, without requiring any moving parts. Particulate matter 60 in the air is entrained within the airflow 50 and also moves towards the second electrodes 30. Much of the particulate matter is electrostatically attracted to the surfaces of the second electrodes, where it remains, thus conditioning the flow of air exiting system 10. Further, the high voltage field present between the electrode arrays can release ozone into the ambient environment, which can eliminate odors that are entrained in the airflow.


In the particular embodiment of FIG. 1A, first electrodes 20 are circular in cross-section, having a diameter of about 0.003″ (0.08 mm), whereas the second electrodes 30 are substantially larger in area and define a “teardrop” shape in cross-section. The ratio of cross-sectional radii of curvature between the bulbous front nose of the second electrode and the first electrodes exceeds 10:1. As shown in FIG. 1A, the bulbous front surfaces of the second electrodes face the first electrodes, and the somewhat “sharp” trailing edges face the exit direction of the airflow. The “sharp” trailing edges on the second electrodes promote good electrostatic attachment of particulate matter entrained in the airflow.


In another particular embodiment shown herein as FIG. 1B, second electrodes 30 are symmetrical and elongated in cross-section. The elongated trailing edges on the second electrodes provide increased area upon which particulate matter entrained in the airflow can attach.


While the electrostatic techniques disclosed by the '801 patent are advantageous over conventional electric fan-filter units, further increased air transport-conditioning efficiency would be advantageous.


SUMMARY

The present invention provides such an apparatus.


One aspect of the present invention is to provide an electro-kinetic air transporter-conditioner that produces an enhanced airflow velocity, enhanced particle collection, and an appropriate amount of ozone production.


An embodiment includes one or more focus or leading electrodes. Each focus or leading electrode may be located upstream to, or even with, each first electrode. The focus or leading electrodes assists in controlling the flow of ionized particles within the airflow. The focus or leading electrode shapes the electrostatic field generated by each first electrode within the electrode assembly.


Another embodiment includes one or more trailing electrodes. Each trailing electrode can be located downstream of a second electrode. The trailing electrode can assist in neutralizing the amount of ions exiting this embodiment of the invention, and can further assist in collecting ionized particles. The trailing electrode can alternatively enhance the flow of negative ions from the transporter-conditioner. Additionally, the trailing electrodes can improve the laminar flow properties of the airflow exiting the air transporter-conditioner.


Another embodiment of the invention includes at least one interstitial electrode located between two second electrodes. The interstitial electrode can also assist in the collection of particulate matter by the second electrodes.


In yet another embodiment of the invention, one or more of the second electrodes are formed to have an enhanced protective end or trailing surface which assists in the operation and cleaning of the embodiment.


In still a further embodiment of the invention, one or more first electrode are of enhanced length in order to increase the emissivity of the first electrode.


Other objects, aspects, features and advantages of the invention will appear from the following description in which the preferred embodiments have been set forth in detail, in conjunction with the accompanying drawings and also from the following claim.





BRIEF DESCRIPTION OF THE DRAWINGS


FIGS. 1A-1B; FIG. 1A is a plan, cross-sectional view, of a first embodiment of an electro-kinetic air transporter-conditioner system according to the prior art; FIG. 1B is a plan, cross-sectional view, of a second embodiment of an electro-kinetic air transporter-conditioner system according to the prior art;



FIGS. 2A-2B; FIG. 2A is a perspective view of a typical embodiment of the housing of an electro-kinetic air transporter-conditioner; FIG. 2B is a perspective view of the embodiment shown in FIG. 2A illustrating the removable second electrodes;



FIG. 3 is an electrical block diagram of the present invention;



FIGS. 4A-4F; FIG. 4A is a perspective view showing an embodiment of an electrode assembly according to the present invention; FIG. 4B is a plan view of the embodiment illustrated in FIG. 4A; FIG. 4C is a perspective view showing another embodiment of an electrode assembly according to the present invention; FIG. 4D is a plan view illustrating a modified version of the embodiment of FIG. 4C; FIG. 4E is a perspective view showing yet another embodiment of an electrode assembly according to the present invention; FIG. 4F is a plan view of the embodiment of FIG. 4E;



FIGS. 5A-5B; FIG. 5A is a perspective view of still another embodiment of the present invention illustrating the leading or focus electrode added to the embodiment shown in FIG. 4A; FIG. 5B is a plan view of a modified embodiment of the present invention similar to that shown in FIG. 5A illustrating a protective end on each second electrode;



FIGS. 6A-6D; FIG. 6A is a perspective view of a further embodiment of the present invention, illustrating a leading or focus electrode added to the embodiment shown in FIG. 4C; FIG. 6B is a perspective view of a modified embodiment of the present invention as shown in FIG. 6A; FIG. 6C is a perspective view of a modified embodiment of the present invention as shown in FIG. 6B; FIG. 6D is a modified embodiment of the present invention, illustrating a leading or focus electrode added to the embodiment in FIG. 4D;



FIGS. 7A-7C; FIG. 7A is a perspective view of another embodiment of the present invention, illustrating a leading or focus electrode added to the embodiment shown in FIG. 4E; FIG. 7B is a perspective view of an embodiment modified from that shown in FIG. 7A; FIG. 7C is a perspective view of an embodiment modified from that shown in FIG. 7B;



FIGS. 8A-8C; FIG. 8A is a perspective view of still a further embodiment of the present invention, illustrating another embodiment of the leading or focus electrode; FIG. 8B is a perspective view of an embodiment modified from that shown in FIG. 5A; FIG. 8C is a perspective view of yet another embodiment;



FIGS. 9A-9C; FIG. 9A is a perspective view of a further embodiment of the present invention; FIG. 9B is a partial view of an embodiment modified from that shown in FIG. 9A; FIG. 9C is another embodiment modified from that shown in FIG. 9A;



FIGS. 10A-10D, FIG. 10A is a perspective view of another embodiment of the present invention, illustrating a trailing electrode added to the embodiment in FIG. 7A; FIG. 10B is a plan view of the embodiment shown in FIG. 10A; FIG. 10C is a plan view of a further embodiment of the present invention; FIG. 10D is a plan view of another embodiment of the present invention similar to FIG. 10C.



FIGS. 11A-11F; FIG. 11A is a plan view of still another embodiment of the present invention; FIG. 11B is a plan view of an embodiment modified from that shown in FIG. 11A; FIG. 11C is a plan view of a further embodiment of the present invention; FIG. 11D is a plan view of an embodiment modified from that shown in FIG. 11C; FIG. 11E is a plan view of a further embodiment of the present invention; FIG. 11F is a plan view of an embodiment modified from that shown in FIG. 11E; and



FIGS. 12A-12C; FIG. 12A is a perspective view of still another embodiment of the present invention; FIG. 12B is a perspective view of a further embodiment of the present invention; FIG. 12C is a perspective view of yet another embodiment of the present invention.



FIG. 13A is a perspective view of an electrode assembly depicting a first embodiment of a mechanism to clean first electrode array electrodes, according to the present invention;



FIG. 13B is a side view depicting an electrode cleaning mechanism as shown in FIG. 13A, according to the present invention;



FIG. 13C is a plan view of the electrode cleaning mechanism shown in FIG. 13B, according to the present invention;



FIG. 14A is a perspective view of a pivotable electrode cleaning mechanism, according to the present invention;



FIGS. 14B-14D depict the cleaning mechanism of FIG. 14A in various positions, according to the present invention;



FIGS. 15A-15E depict cross-sectional views of bead-like mechanisms to clean first electrode array electrodes, according to the present invention.





DESCRIPTION OF THE PREFERRED EMBODIMENT(S)

Overall Air-Transporter Conditioner System Configuration:



FIGS. 2A and 2B depict an electro-kinetic air transporter-conditioner system 100 whose housing 102 includes preferably rear-located intake vents or louvers 104 and preferably front located exhaust vents 106, and a base pedestal 108. If desired a single vent can provide and be used as both an air intake and an air exhaust with an air inlet channel and an air exhaust channel communicating with the vent and the electrodes. Preferably the housing is freestanding and/or upstandingly vertical and/or elongated. Internal to the transporter housing is anion generating unit 160, preferably powered by an AC:DC power supply that is energizable or excitable using switch S1. S1, which along with the other below described user operated switches are conveniently located at the top 103 of the unit 100. Ion generating unit 160 is self-contained in that other ambient air, nothing is required from beyond the transporter housing, save external operating potential, for operation of the present invention.


The upper surface of housing 102 includes a user-liftable handle member 112 to which is affixed a second array 240 of collector electrodes 242 within an electrode assembly 220. Electrode assembly 220 also comprises a first array of emitter electrodes 230, or a single first electrode shown here as a single wire or wire-shaped electrode 232. (The terms “wire” and “wire-shaped” shall be used interchangeably herein to mean an electrode either made from a wire or, if thicker or stiffer than a wire, having the appearance of a wire.) In the embodiment shown, lifting member 112 lifts second array electrodes 240 upward, causing the second electrode to telescope out of the top of the housing and, if desired, out of unit 100 for cleaning, while the first electrode way 230 remains within unit 100. As is evident from the figure, the second array of electrode can be lifted vertically out from the top 103 of unit 100 along the longitudinal axis or direction of the elongated housing 102. This arrangement with the second electrodes removable from the top 103 of the unit 100, makes it easy for the user to pull the second electrodes out for cleaning. In FIG. 2B, the bottom ends of second electrodes 242 are connected to a member 113, to which is attached a mechanism 500, which includes a flexible member and a slot for capturing and cleaning the first electrode 232, whenever handle member 112 is moved upward or downward by a user.


The first and second arrays of electrodes are coupled to the output terminals of ion generating unit 160, as best seen in FIG. 3.


The general shape of the embodiment of the invention shown in FIGS. 2A and 2B is that of a figure eight in cross-section, although other shapes are within the spirit and scope of the invention. The top-to-bottom height of the preferred embodiment is in one preferred embodiment, 1 m, with a left-to-right width of preferably 15 cm, and a front-to-back depth of perhaps 10 cm, although other dimensions and shapes can of course be used. A louvered construction provides ample inlet and outlet venting in an economical housing configuration. There need be no real distinction between vents 104 and 106, except their location relative to the second electrodes. These vents serve to ensure that an adequate flow of ambient air can be drawn into or made available to the unit 100, and that an adequate flow of ionized air that includes appropriate amounts of O3 flows out from unit 100.


As will be described, when unit 100 is energized with S1, high voltage or high potential output by ion generator 160 produces ions at the first electrode, which ions are attracted to the second electrodes. The movement of the ions in an “IN” to “OUT” direction carries with the ions air molecules, thus electro-kinetically producing an outflow of ionized air. The “IN” notation in FIGS. 2A and 2B denote the intake of ambient air with particulate matter 60. The “OUT” notation in the figures denotes the outflow of cleaned air substantially devoid of the particulate matter, which particulates matter adheres electrostatically to the surface of the second electrodes. In the process of generating the ionized airflow appropriate amounts of ozone (O3) are beneficially produced. It may be desired to provide the inner surface of housing 102 with an electrostatic shield to reduces detectable electromagnetic radiation. For example, a metal shield could be disposed within the housing, or portions of the interior of the housing can be coated with a metallic paint to reduce such radiation.


The housing preferably has a substantially oval-shaped or -elliptically shaped cross-section with dimpled side grooves. Thus, as indicated above, the cross-section looks somewhat like a figure eight. It is within the scope of the present invention for the housing to have a different shaped cross-section such as, but not limited to, a rectangular shape, an egg shape, a tear-drop shape, or circular shape. The housing preferably has a tall, thin configuration. As will become apparent later, the housing is preferably functionally shaped to contain the electrode assembly.


As mentioned above, the housing has an inlet and an outlet. Both the inlet and the outlet are covered by fins or louvers. Each fin is a thin ridge spaced-apart from the next fin, so that each fin creates minimal resistance as air flows through the housing. The fins are horizontal and are directed across the elongated vertical upstanding housing of the unit. Thus, the fins are substantially perpendicular in this preferred embodiment to the electrodes. The inlet and outlet fins are aligned to give the unit a “see through” appearance. Thus, a user can “see through” the unit from the inlet to the outlet. The user will see no moving parts within the housing, but just a quiet unit that cleans the air passing therethrough. Alternatively the fins can be parallel with the electrodes in another preferred embodiment. Other orientations of fins and electrodes are possible in other embodiments.


As best seen in FIG. 3, ion generating unit 160 includes a high voltage generator unit 170 and circuitry 180 for converting raw alternating voltage (e.g., 117 VAC) into direct current (“DC”) voltage. Circuitry 180 preferably includes circuitry controlling the shape and/or duty cycle of the generator unit output voltage (which control is altered with user switch S2). Circuitry 180 preferably also includes a pulse mode component, coupled to switch S3, to temporarily provide a burst of increased output ozone. Circuitry 180 can also include a timer circuit and a visual indicator such as a light emitting diode (“LED”). The LED or other indicator (including, if desired, an audible indicator) signals when ion generation quits occurring. The timer can automatically halt generation of ions and/or ozone after some predetermined time, e.g., 30 minutes.


The high voltage generator unit 170 preferably comprises a low voltage oscillator circuit 190 of perhaps 20 KHz frequency, that outputs low voltage pulses to an electronic switch 200, e.g., a thyristor or the like. Switch 200 switchably couples the low voltage pulses to the input winding of a step-up transformer T1. The secondary winding of T1 is coupled to a high voltage multiplier circuit 210 that outputs high voltage pulses. Preferably the circuitry and components comprising high voltage pulse generator 170 and circuit 180 are fabricated on a printed circuit board that is mounted within housing 102. If desired, external audio input (e.g., from a stereo tuner) could be suitably coupled to oscillator 190 to acoustically modulate the kinetic airflow produced by unit 160. The result would be an electrostatic loudspeaker, whose output airflow is audible to the human ear in accordance with the audio input signal. Further, the output air stream would still include ions and ozone.


Output pulses from high voltage generator 170 preferably are at least 10 KV peak-to-peak with an effective DC offset of, for example, half the peak-to-peak voltage, and have a frequency of, for example, 20 KHz. Frequency of oscillation can include other values, but frequency of at least about 20 KHz is preferred as being inaudible to humans. If pets will be in the same room as the unit 100, it may be desired to utilize and even higher operating frequency, to prevent pet discomfort and/or howling by the pet. The pulse train output preferably has a duty cycle of for example 10%, which will promote battery lifetime if live current is not used. Of course, different peak-peak amplitudes, DC offsets, pulse train waveshapes, duty cycle, and/or repetition frequencies can be used instead. Indeed, a 100% pulse train (e.g., an essentially DC high voltage) may be used, albeit with shorter battery lifetime. Thus, generator unit 170 for this embodiment can be referred to as a high voltage pulse generator. Unit 170 functions as a DC:DC high voltage generator, and could be implemented using other circuitry and/or techniques to output high voltage pulses that are input to electrode assembly 220.


As noted, outflow (OUT) preferably includes appropriate amounts of ozone that can remove odors and preferably destroy or at least substantially alter bacteria, germs, and other living (or quasi-living) matter subjected to the outflow. Thus, when switch S2 is closed and the generator 170 has sufficient operating potential, pulses from high voltage pulse generator unit 170 create an outflow (OUT) of ionized air and ozone. When S1 is closed, LED will visually signal when ionization is occurring.


Preferably operating parameters of unit 100 are set during manufacture and are generally not user-adjustable. For example, with respect to operating parameters, increasing the peak-to-peak output voltage and/or duty cycle in the high voltage pulses generated by unit 170 can increase the airflow rate, ion content, and ozone content. These parameters can be set by the user by adjusting switch S2 as disclosed below. In the preferred embodiment, output flowrate is about 200 feet/minute, ion content is about 2,000,000/cc and ozone content is about 40 ppb (over ambient) to perhaps 2,000 ppb (over ambient). Decreasing the ratio of the radius of the nose of the second electrodes to the radius of the first electrode or decreasing the ratio of the cross-sectioned area of the second electrode to the first electrode below about 20:1 will decrease flow rate, as will decreasing the peak-to-peak voltage and/or duty cycle of the high voltage pulses coupled between the first and second electrode arrays.


In practice, unit 100 is placed in a room and connected to an appropriate source of operating potential, typically 117 VAC. With S1 energizing ionization unit 160, systems 100 emits ionized air and preferably some ozone via outlet vents 106. The airflow, coupled with the ions and ozone freshens the air in the room, and the ozone can beneficially destroy or at least diminish the undesired effects of certain odors, bacteria, germs, and the like. The airflow is indeed electro-kinetically produced, in that there are no intentionally moving parts within unit 100. (Some mechanical vibration may occur within the electrodes).


Having described various aspects of this embodiment of the invention in general, preferred embodiments of electrode assembly 220 are now described. In the various embodiments, electrode assembly 220 comprises a first array 230 of at least one electrode or conductive surface 232, and further comprises a second array 240 of preferably at least one electrode or conductive surface 242. Understandably material(s) for electrodes 232 and 242 should conduct electricity, be resistant to corrosive effects from the application of high voltage, yet be strong enough to be cleaned.


In the various electrode assemblies to be described herein, electrode(s) 232 in the first electrode array 230 are preferably fabricated from tungsten. Tungsten is sufficiently robust in order to withstand cleaning, has a high melting point to retard breakdown due to ionization, and has a rough exterior surface that seems to promote efficient ionization. On the other hand, electrode(s) 242 preferably have a highly polished exterior surface to minimize unwanted point-to-point radiation. As such, electrode(s) 242 preferably are fabricated from stainless steel and/or brass, among other materials. The polished surface of electrode(s) 232 also promotes ease of electrode cleaning.


In contrast to the prior art electrodes disclosed by the '801 patent, electrodes 232 and 242, are light weight, easy to fabricate, and lend themselves to mass production. Further, electrodes 232 and 242 described herein promote more efficient generation of ionized air, and appropriate amounts of ozone, (indicated in several of the figures as O3).


Electrode Assembly with First and Second Electrodes:



FIGS. 4A-4F



FIGS. 4A-4F illustrate various configurations of the electrode assembly 220. The output from high voltage pulse generator unit 170 is coupled to an electrode assembly 220 that comprises a first electrode array 230 and a second electrode array 240. Again, instead of arrays, single electrodes or single conductive surfaces can be substituted for one or both array 230 and array 240.


The positive output terminal of unit 170 is coupled to first electrode array 230, and the negative output terminal is coupled to second electrode array 240. It is believed that with this arrangement the net polarity of the emitted ions is positive, e.g., more positive ions than negative ions are emitted. This coupling polarity has been found to work well, including minimizing unwanted audible electrode vibration or hum. However, while generation of positive ions is conducive to a relatively silent airflow, from a health standpoint, it is desired that the output airflow be richer in negative ions, not positive ions. It is noted that in some embodiments, one port (preferably the negative port) of the high voltage pulse generator can in fact be the ambient air. Thus, electrodes in the second array need not be connected to the high voltage pulse generator using a wire. Nonetheless, there will be an “effective connection” between the second array electrodes and one output port of the high voltage pulse generator, in this instance, via ambient air. Alternatively the negative output terminal of unit 170 can be connected to the first electrode array 230 and the positive output terminal can be connected to the second electrode array 240.


With this arrangement an electrostatic flow of air is created, going from the first electrode array towards the second electrode array. (This flow is denoted “OUT” in the figures.) Accordingly electrode assembly 220 is mounted within transporter system 100 such that second electrode array 240 is closer to the OUT vents and first electrode array 230 is closer to the IN vents.


When voltage or pulses from high voltage pulse generator 170 are coupled across first and second electrode arrays 230 and 240, a plasma-like field is created surrounding electrodes 232 in first array 230. This electric field ionizes the ambient air between the first and second electrode arrays and establishes an “OUT” airflow that moves towards the second array. It is understood that the IN flow enters via vent(s) 104, and that the OUT flow exits via vent(s) 106.


Ozone and ions are generated simultaneously by the first array electrodes 232, essentially as a function of the potential from generator 170 coupled to the first array of electrodes or conductive surfaces. Ozone generation can be increased or decreased by increasing or decreasing the potential at the first array. Coupling an opposite polarity potential to the second array electrodes 242 essentially accelerates the motion of ions generated at the first array, producing the airflow denoted as “OUT” in the figures. As the ions and ionized particulates move toward the second array, the ions and ionized particles push or move air molecules toward the second array. The relative velocity of this motion may be increased, by way of example, by decreasing the potential at the second array relative to the potential at the first array.


For example, if +10 KV were applied to the first array electrode(s), and no potential were applied to the second array electrode(s), a cloud of ions (whose net charge is positive) would form adjacent the first electrode array. Further, the relatively high 10 KV potential would generate substantial ozone. By coupling a relatively negative potential to the second array electrode(s), the velocity of the air mass moved by the net emitted ions increases.


On the other hand, if it were desired to maintain the same effective outflow (OUT) velocity, but to generate less ozone, the exemplary 10 KV potential could be divided between the electrode arrays. For example, generator 170 could provide +4 KV (or some other fraction) to the first array electrodes and −6 KV (or some other fraction) to the second array electrodes. In this example, it is understood that the +4 KV and the −6 KV are measured relative to ground. Understandably it is desired that the unit 100 operates to output appropriate amounts of ozone. Accordingly, the high voltage is preferably fractionalized with about +4 KV applied to the first array electrodes and about −6 KV applied to the second array electrodes.


In the embodiments of FIGS. 4A and 4B, electrode assembly 220 comprises a first array 230 of wire-shaped electrodes 232, and a second array 240 of generally “U”-shaped electrodes 242. In preferred embodiments, the number N1 of electrodes comprising the first array can preferably differ by one relative to the number N2 of electrodes comprising the second array 240. In many of the embodiments shown, N2>N1. However, if desired, additional first electrodes 232 could be added at the outer ends of array 230 such that N1>N2, e.g., five first electrodes 232 compared to four second electrodes 242.


As previously indicated first or emitter electrodes 232 are preferably lengths of tungsten wire, whereas electrodes 242 are formed from sheet metal, preferably stainless steel, although brass or other sheet metal could be used. The sheet metal is readily configured to define side regions 244 and bulbous nose region 246, forming the hollow, elongated “U”-shaped electrodes 242. While FIG. 4A depicts four electrodes 242 in second array 240 and three electrodes 232 in first array 230, as noted previously, other numbers of electrodes in each array could be used, preferably retaining a symmetrically staggered configuration as shown. It is seen in FIG. 4A that while particulate matter 60 is present in the incoming (IN) air, the outflow (OUT) air is substantially devoid of particulate matter, which adheres to the preferably large surface area provided by the side regions 244 of the second array electrodes 242.



FIG. 4B illustrates that the spaced-apart configuration between the first and second arrays 230, 240 is staggered. Preferably, each first array electrode 232 is substantially equidistant from two second array electrodes 242. This symmetrical staggering has been found to be an efficient electrode placement. Preferably, in this embodiment, the staggering geometry is symmetrical in that adjacent electrodes 232 or adjacent electrodes 242 are spaced-apart a constant distance, Y1 and Y2 respectively. However, a non-symmetrical configuration could also be used. Also, it is understood that the number of electrodes 232 and 242 may differ from what is shown.


In the embodiment of FIG. 4A, typically dimensions are as follows: diameter of electrodes 232, R1, is about 0.08 mm, distances Y1 and Y2 are each about 16 mm, distance X1 is about 16 mm, distance L is about 20 mm, and electrode heights Z1 and Z2 are each about 1 m. The width W of electrodes 242 is preferably about 4 mm, and the thickness of the material from which electrodes 242 are formed is about 0.5 mm. Of course other dimensions and shapes could be used. For example, preferred dimensions for distance X1 may vary between 12-30 mm, and the distance Y2 may vary between 15-30 mm. It is preferred that electrodes 232 have a small diameter. A wire having a small diameter, such as R1, generates a high voltage field and has a high emissivity. Both characteristics are beneficial for generating ions. At the same time, it is desired that electrodes 232 (as well as electrodes 242) be sufficiently robust to withstand occasional cleaning.


Electrodes 232 in first array 230 are coupled by a conductor 234 to a first (preferably positive) output port of high voltage pulse generator 170. Electrodes 242 in second array 240 are coupled by a conductor 249 to a second (preferably negative) output port of high voltage generator 170. The electrodes may be electrically connected to the conductors 234 or 249 at various locations. By way of example only, FIG. 4B depicts conductor 249 making connection with some electrodes 242 internal to bulbous end 246, while other electrodes 242 make electrical connection to conductor 249 elsewhere on the electrode 242. Electrical connection to the various electrodes 242 could also be made on the electrode external surface, provided no substantial impairment of the outflow airstream results; however it has been found to be preferable that the connection is made internally.


In this and the other embodiments to be described herein, ionization appears to occur at the electrodes 232 in the first electrode array 230, with ozone production occurring as a function of high voltage arcing. For example, increasing the peak-to-peak voltage amplitude and/or duty cycle of the pulses from the high voltage pulse generator 170 can increase ozone content in the output flow of ionized air. If desired, user-control S2 can be used to somewhat vary ozone content by varying amplitude and/or duty cycle. Specific circuitry for achieving such control is known in the art and need not be described in detail herein.


Note the inclusion in FIGS. 4A and 4B of at least one output controlling electrodes 243, preferably electrically coupled to the same potential as the second array electrodes 242. Electrode 243 preferably defines a pointed shape in side profile, e.g., a triangle. The sharp point on electrodes 243 causes generation of substantial negative ions (since the electrode is coupled to relatively negative high potential). These negative ions neutralize excess positive ions otherwise present in the output airflow, such that the OUT flow has a net negative charge. Electrodes 243 is preferably stainless steel, copper, or other conductor material, and is perhaps 20 mm high and about 12 mm wide at the base. The inclusion of one electrode 243 has been found sufficient to provide a sufficient number of output negative ions, but more such electrodes may be included.


In the embodiments of FIGS. 4A, 4B and 4C, each “U”-shaped electrode 242 has two trailing surface or sides 244 that promote efficient kinetic transport of the outflow of ionized air and ozone. For the embodiment of FIG. 4C, there is the inclusion on at least one portion of a trailing edge of a pointed electrode region 243′. Electrode region 243′ helps promote output of negative ions, in the same fashion that was previously described with respect to electrodes 243, as shown in FIGS. 4A and 4B.


In FIG. 4C and the figures to follow, the particulate matter is omitted for ease of illustration. However, from what was shown in FIGS. 4A-4B, particulate matter will be present in the incoming air, and will be substantially absent from the outgoing air. As has been described, particulate matter 60 typically will be electrostatically precipitated upon the surface area of electrodes 242.


As discussed above and as depicted by FIG. 4C, it is relatively unimportant where on an electrode array electrical connection is made. Thus, first array electrodes 232 are shown electrically connected together at their bottom regions by conductor 234, whereas second array electrodes 242 are shown electrically connected together in their middle regions by the conductor 249. Both arrays may be connected together in more than one region, e.g., at the top and at the bottom. It is preferred that the wire or strips or other inter-connecting mechanisms be at the top, bottom, or periphery of the second array electrodes 242, so as to minimize obstructing stream air movement through the housing 210.


It is noted that the embodiments of FIGS. 4C and 4D depict somewhat truncated versions of the second electrodes 242. Whereas dimension L in the embodiment of FIGS. 4A and 4B was about 20 mm, in FIGS. 4C and 4D, L has been shortened to about 8 mm. Other dimensions in FIG. 4C preferably are similar to those stated for FIGS. 4A and 4B. It will be appreciated that the configuration of second electrode array 240 in FIG. 4C can be more robust than the configuration of FIGS. 4A and 4B, by virtue of the shorter trailing edge geometry. As noted earlier, a symmetrical staggered geometry for the first and second electrode arrays is preferred for the configuration of FIG. 4C.


In the embodiment of FIG. 4D, the outermost second electrodes, denoted 242-1 and 242-4, have substantially no outermost trailing edges. Dimension L in FIG. 4D is preferably about 3 mm, and other dimensions may be as stated for the configuration of FIGS. 4A and 4B. Again, the ratio of the radius or surface areas between the first electrode 232 and the second electrodes 242 for the embodiment of FIG. 4D preferably exceeds about 20:1.



FIGS. 4E and 4F depict another embodiment of electrode assembly 220, in which the first electrode array 230 comprises a single wire electrode 232, and the second electrode array 240 comprises a single pair of curved “L”-shaped electrodes 242, in cross-section. Typical dimensions, where different than what has been stated for earlier-described embodiments, are X1≈12 mm, Y2≈5 mm, and L1≈3 mm. The effective surface area or radius ratio is again greater than about 20:1. The fewer electrodes comprising assembly 220 in FIGS. 4E and 4F promote economy of construction, and ease of cleaning, although more than one electrode 232, and more than two electrodes 242 could of course be employed. This particular embodiment incorporates the staggered symmetry described earlier, in which electrode 232 is equidistant from two electrodes 242. Other geometric arrangements, which may not be equidistant, are within the spirit and scope of the invention.


Electrode Assembly with an Upstream Focus Electrode:



FIGS. 5A-5B


The embodiments illustrated in FIGS. 5A-5B are somewhat similar to the previously described embodiments in FIGS. 4A-4B. The electrode assembly 220 includes a first array of electrodes 230 and a second array of electrodes 240. Again, for this and the other embodiments, the term “array of electrodes” may refer to a single electrode or a plurality of electrodes. Preferably, the number of electrodes 232 in the first array of electrodes 230 will differ by one relative to the number of electrodes 242 in the second array of electrodes 240. The distances L, X1, Y1, Y2, Z1 and Z2 for this embodiment are similar to those previously described in FIG. 4A.


As shown in FIG. 5A, the electrode assembly 220 preferably adds a third, or leading, or focus, or directional electrode 224a, 224b, 224c (generally referred to as “electrode 224”) upstream of each first electrode 232-1, 232-2, 232-3. The focus electrode 224 produces an enhanced airflow velocity exiting the devices 100 or 200. In general, the third focus electrode 224 directs the airflow, and ions generated by the first electrode 232, towards the second electrodes 242. Each third focus electrode 224 is a distance X2 upstream from at least one of the first electrodes 232. The distance X2 is preferably 5-6 mm, or four to five diameters of the focus electrode 224. However, the third focus electrode 224 can be further from or closer to the first electrode 232.


The third focus electrode 224 illustrated in FIG. 5A is a rod-shaped electrode. The third focus electrode 224 can also comprise other shapes that preferably do not contain any sharp edges. The third focus electrode 224 is preferably manufactured from material that will not erode or oxidize, such as stainless steel. The diameter of the third focus electrode 224, in a preferred embodiment, is at least fifteen times greater than the diameter of the first electrode 232. The diameter of the third focus electrode 224 can be larger or smaller. The diameter of the third focus electrode 224 is preferably large enough so that third focus electrode 224 does not function as an ion emitting surface when electrically connected with the first electrode 232. The maximum diameter of the third focus electrode 224 is somewhat constrained. As the diameter increases, the third focus electrode 224 will begin to noticeably impair the airflow rate of the units 100 or 200. Therefore, the diameter of the third electrode 224 is balanced between the need to form a non-ion emitting surface and airflow properties of the unit 100 or 200.


In a preferred embodiment, each third focus electrodes 224a, 224b, 224c are electrically connected with the first array 230 and the high voltage generator 170 by the conductor 234. As shown in FIG. 5A, the third focus electrodes 224 are electrically connected to the same positive outlet of the high voltage generator 170 as the first array 230. Accordingly, the first electrode 232 and the third focus electrode 224 generate a positive electric field. Since the electrical fields generated by the third focus electrode 224 and the first electrode 232 are both positive, the positive field generated by the third focus electrode 224 can push, or repel, or direct, the positive field generated by the first electrode 232 towards the second array 240. For example, the positive field generated by the third focus electrode 224a will push, or repel, or direct, the positive field generated by the first electrode 232-1 towards the second array 240. In general, the third focus electrode 224 shapes the electrical field generated by each electrode 232 in the first array 230. This shaping effect is believed to decrease the amount of ozone generated by the electrode assembly 220 and increases the airflow of units 100 and 200.


The particles within the airflow are positively charged by the ions generated by the first electrode 232. As previously mentioned, the positively charged particles are collected by the negatively charged second electrodes 242. The third focus electrode 224 also directs the airflow towards the second electrodes 242 by guiding the charged particles towards the trailing sides 244 of each second electrode 242. It is believed that the airflow will travel around the third focus electrode 224, partially focusing the airflow towards the trailing sides 244, improving the collection rate of the electrode assembly 220.


The third focus electrode 224 may be located at various positions upstream of each first electrode 232. By way of example only, a third focus electrode 224b is located directly upstream of the first electrode 232-2 so that the center of the third focus electrode 224b is in-line and symmetrically aligned with the first electrode 232-2, as shown by extension line B. Extension line B is located midway between the second electrode 242-2 and the second electrode 242-3.


Alternatively, a third focus electrode 224 can also be located at an angle relative to the first electrode 232. For example, a third focus electrode 224a can be located upstream of the first electrode 232-1 along a line extending from the middle of the nose 246 of the second electrode 242-2 through the center of the first electrode 232-1, as shown by extension line A. The third focus electrode 224a is in-line and symmetrically aligned with the first electrode 232-1 along extension line A. Similarly, the third electrode 224c is located upstream to the first electrode 232-3 along a line extending from the middle of the nose 246 of the second electrode 242-3 through the first electrode 232-3, as shown by extension line C. The third focus electrode 224c is in-line and symmetrically aligned with the first electrode 232-3 along extension line C. It is within the scope of the present invention for the electrode assembly 220 to include third focus electrodes 224 that are both directly upstream and at an angle to the first electrodes 232, as depicted in FIG. 5A. Thus the focus electrodes fan out relating to the first electrodes.



FIG. 5B illustrates that an electrode assembly 220 may contain multiple third focus electrodes 224 upstream of each first electrode 232. By way of example only, the third focus electrode 224a2 is in-line and symmetrically aligned with the third focus electrode 224a1, as shown by extension line A. In a preferred embodiment, only the third focus electrodes 224a1, 224b1, 224c1 are electrically connected to the high voltage generator 170 by conductor 234. Accordingly, not all of the third electrodes 224 are at the same operating potential. In the embodiment shown in FIG. 5B, the third focus electrodes 224a1, 224b1, 224c1 are at the same electrical potential as the first electrodes 232, while the third focus electrodes 224a2, 224b2, 224c2 are floating. Alternatively, the third focus electrodes 224a2, 224b2 and 224c2 may be electrically connected to the high voltage generator 170 by the conductor 234.



FIG. 5B illustrates that each second electrode 242 may also have a protective end 241. In the previous embodiments, each “U”-shaped second electrode 242 has an open end. Typically, the end of each trailing side or side wall 244 contains sharp edges. The gap between the trailing sides or side walls 244, and the sharp edges at the end of the trailing sides or side walls 244, generate unwanted eddy currents. The eddy currents create a “backdraft,” or airflow traveling from the outlet towards the inlet, which slow down the airflow rate of the units 100 or 200.


In a preferred embodiment, the protective end 241 is created by shaping, or rolling, the trailing sides or side walls 244 inward and pressing them together, forming a rounded trailing end with no gap between the trailing sides or side walls of each second electrode 242. Accordingly, the side walls have outer surfaces, and the outer surface of the end of side walls are bent back adjacent to the trailing ends of the side walls so that the outer surface of the side walls are adjacent to, or face, or touch each other. Accordingly a smooth trailing edge is integrally formed on the second electrode. If desired, it is within the scope of the invention to spot weld the rounded ends together along the length of the second electrode 242. It is also within the scope of the present invention to form the protective end 241 by other methods such as, but not limited to, placing a strap of plastic across each end of the trailing sides 244 for the full length of the second electrode 242. The rounded or capped end is an improvement over the previous electrodes 242 without a protective end 241. Eliminating the gap between the trailing sides 244 also reduces or eliminates the eddy currents typically generated by the second electrode 242. The rounded protective end also provides a smooth surface for the purpose of cleaning the second electrode. Accordingly in this embodiment the collector electrode is a one-piece, integrally formed, electrode with a protection end.



FIGS. 6A-6D



FIG. 6A illustrates an electrode assembly 220 including a first array of electrodes 230 having three wire-shaped first electrodes 232-1, 232-2, 232-3 (generally referred to as “electrode 232”) and a second array of electrodes 240 having four “U”-shaped second electrodes 242-1, 242-2, 242-3, 242-4 (generally referred to as “electrode 242”). Each first electrode 232 is electrically connected to the high voltage generator 170 at the bottom region, whereas each second electrode 242 is electrically connected to the high-voltage generator 170 in the middle to illustrate that the first and second electrodes 232, 242 can be electrically connected in a variety of locations.


The second electrode 242 in FIG. 6A is a similar version of the second electrode 242 shown in FIG. 4C. The distance L has been shortened to about 8 mm, while the other dimensions X1, Y1, Y2, Z1, Z2 are similar to those shown in FIG. 4A.


A third leading or focus electrode 224 is located upstream of each first electrode 232. The innermost third focus electrode 224b is located directly upstream of the first electrode 232-2, as shown by extension line B. Extension line B is located midway between the second electrodes 242-2, 242-3. The third focus electrodes 224a, 224c are at an angle with respect to the first electrodes 232-1, 232-3. For example, the third focus electrode 224a is upstream to the first electrode 232-1 along a line extending from the middle of the nose 246 of the second electrode 242-2 extending through the center of the first electrode 232-1, as shown by extension line A. The third electrode 224c is located upstream of the first electrode 232-3 along a line extending from the center of the nose 246 of the second electrode 242-3 through the center of the first electrode 232-3, as shown by extension line C. Accordingly and preferably the focus electrodes fan out relative to the first electrodes as an aid for directing the flow of ions and charged particles. FIG. 6B illustrates that the third focus electrodes 224 and the first electrode 232 may be electrically connected to the high voltage generator 170 by conductor 234.



FIG. 6C illustrates that a pair of third focus electrodes 224 may be located upstream of each first electrode 232. Preferably, the multiple third focus electrodes 224 are in-line and symmetrically aligned with each other. For example, the third focus electrode 224a2 is in-line and symmetrically aligned with the third focus electrode 224a1, along extension line A. As previously mentioned, preferably only third focus electrodes 224a1, 224b1, 224c1 are electrically connected with the first electrodes 232 by conductor 234. It is also within the scope of the present invention to have none or all of the third focus electrodes 224 electrically connected to the high voltage generator 170.



FIG. 6D illustrates third focus electrodes 224 added to the electrode assembly 220 shown in FIG. 4D. Preferably, a third focus electrode 224 is located upstream of each first electrode 232. For example, the third focus electrode 224b is in-line and symmetrically aligned with the first electrode 232-2, as shown by extension line B. Extension line B is located midway between the second electrodes 242-2, 242-3. The third focus electrode 224a is in-line and symmetrically aligned with the first electrode 232-1, as shown by extension line A. Similarly, the third electrode 224c is in-line and symmetrically aligned with the first electrode 232-3, as shown by extension line C. Extension lines A-C extend from the middle of the nose 246 of the “U”-shaped second electrodes 242-2, 242-3 through the first electrodes 232-1, 232-3, respectively. In a preferred embodiment, the third electrodes 224a, 224b, 224c with the high voltage generator 170 by the conductor 234. This embodiment can also include a pair of third focus electrodes 224 upstream of each first electrode 232 as is depicted in FIG. 6C.



FIGS. 7A-7C



FIGS. 7A-7C illustrate that the electrode assembly 220 shown in FIG. 4E can include a third focus electrode upstream of the first array of electrodes 230 comprising a single wire electrode 232. Preferably, the center of the third focus electrode 224 is in-line and symmetrically aligned with the center of the first electrode 232, as shown by extension line B. Extension line B is located midway between the second electrodes 242. The distances X1, X2, Y1, Y2, Z1 and Z2 are similar to the embodiments previously described. The first electrode 232 and the second electrode 242 may be electrically connected to the high-voltage generator 170 by conductor 234, 249 respectively. It is within the scope of the present invention to connect the first and second electrodes to opposite ends of the high voltage generator 170 (e.g., the first electrode 232 may be negatively charged and the second electrode 242 may be positively charged). In a preferred embodiment the third focus electrode 224 is also electrically connected to the high voltage generator 170.



FIG. 7B illustrates that a pair of third focus electrodes 224a, 224b may be located upstream of the first electrode 232. The third focus electrodes 224a, 224b are in-line and symmetrically aligned with the first electrode 232, as shown by extension line B. Extension line B is located midway between the second electrodes 242. Preferably, the third focus electrode 224b is upstream of third focus electrode 224a a distance equal to the diameter of a third focus electrode 224. In a preferred embodiment, only the third focus electrode 224a is electrically connected to the high voltage generator 170. It is within the scope of the present invention to electrically connect both third focus electrodes 224a, 224b to the high voltage generator 170.



FIG. 7C illustrates that each third focus electrode 224 can be located at an angle with respect to the first electrode 232. Similar to the previous embodiments, the third focus electrode 224a1 and 224b1 is located a distance X2 upstream from the first electrode 232. By way of example only, the third focus electrodes 224a1, 224a2 are located along a line extending from the middle of the second electrode 242-2 through the center of the first electrode 232, as shown by extension line A. Similarly, the third focus electrodes 224b1, 224b2 are along a line extending from the middle of the second electrode 242-1 through the middle of the first electrode 232, as shown by extension line B. The third focus electrode 224a2 is in-line and symmetrically aligned with the third focus electrode 224a1 along extension line A. Similarly, the third focus electrode 224b2 is in line and symmetrically aligned with the third focus electrode 224b1 along extension line B. The third focus electrodes 224 are fanned out and form a “V” pattern upstream of first electrode 232. In a preferred embodiment, only the third focus electrodes 224a1 and 224b1 are electrically connected to the high-voltage generator 170 by conductor 234. It is within the scope of the invention to electrically connect the third focus electrodes 224a and 224b2 to the high voltage generator 170.



FIGS. 8A-8B


The previously described embodiments of the electrode assembly 220 disclose a rod-shaped third focus electrode 224 upstream of each first electrode 232. FIG. 8A illustrates an alternative configuration for the third focus electrode 224. By way of example only, the electrode assembly 220 may include a “U”-shaped or possibly “C”-shaped third focus electrode 224 upstream of each first electrode 232. Further the third focus electrode 224 can have other curved configurations such as, but not limited to, circular-shaped, elliptical-shaped, and parabolically-shaped other concave shapes facing the first electrode 232. In a preferred embodiment, the third focus electrode 224 has holes 225 extending through, forming a perforated surface to minimize the resistance of the third focus electrode 224 on the airflow rate.


In a preferred embodiment, the third focus electrode 224 is electrically connected to the high voltage generator 170 by conductor 234. The third focus electrode 224 in FIG. 8A is preferably not an ion emitting surface. Similar to previous embodiments, the third focus electrode 224 generates a positive electric field and pushes or repels the electric field generated by the first electrode 232 towards the second array 240.



FIG. 8B illustrates that a perforated “U”-shaped or “C”-shaped third focus electrode 224 can be incorporated into the electrode assembly 220 shown in FIG. 4A. Even though only two configurations of the electrode assembly 220 are shown with the perforated “U”-shaped third focus electrode 224, all the embodiments described in FIGS. 5A-12C may incorporate the perforated “U”-shaped third focus electrode 224. It is also within the scope of the invention to have multiple perforated “U”-shaped third focus electrodes 224 upstream of each first electrode 232. Further in other embodiment the “U”-shaped third focus electrode 224 can be made of a screen or a mesh.



FIG. 8C illustrates third focus electrodes 224 similar to those depicted in FIG. 8B, except that the third focus electrodes 224 are rotated by 180 degree. to preset a convex surface facing to the first electrodes 232 in order to focus and direct the field of ions and airflow from the first electrode 232 toward the second electrode 242. These third focus electrodes 224 shown in FIGS. 8A-8C are located along extension lines A, B, C similar to previously described embodiments.



FIGS. 9A-9C



FIG. 9A illustrates a pin-ring configuration of the electrode assembly 220. The electrode assembly 220 contains a cone-shaped or triangular-shaped first electrode 232, a ring-shaped second electrode 242 downstream of the first electrode 232, and a third focus electrode 250 upstream of the first electrode 232. The third focus electrodes 250 may be electrically connected to the high voltage generator 170. Preferably the focus electrode 250 is spaced from the first electrode 232 a distance that is in accordance with the other embodiments described herein. Alternatively, the third focus electrode 250 can have a floating potential. As indicated by phantom elements 232′, 242′, the electrode assembly 220 can comprise a plurality of such pin-like and ring-like elements. The plurality of pin-ring configurations as depicted in FIG. 9A can be positioned one above the other along the elongated housing of the invention. Such a plurality of pin-ring configurations can of course operate in another embodiment without the third focus electrode. It is understood that this plurality of pin-ring configurations can be upstanding and elongated along the elongated direction of said housing and can replace the first and second electrodes shown, for example, in FIG. 2B and be removable much as the second electrode in FIG. 2B is removable. Preferably, the first electrode 232 is tungsten, and the second electrode 242 is stainless steel. Typical dimensions for the embodiment of FIG. 9A are L1≈10 millimeters, X1≈9.5 millimeters, T≈0.5 millimeters and the diameter of the opening 246≈12 millimeters.


The electrical properties and characteristics of the third focus electrode 250 is similar to the third focus electrode 224 described in previous embodiments. In contrast to the rod-shaped physical characteristic of the previous embodiments, the shape the third focus electrode 250 is a concave disc, with the concave surface preferably facing toward the second electrodes 242. The third focus electrode 250 preferably has holes extending therethrough to minimize the disruption in airflow. It is within the scope of the present invention for the third focus electrode 250 to comprise other shapes such as, but not limited to, a convex disc a parabolic disc, a spherical disc, or other convex or concave shapes or a rectangle, or other planar surface and be within the spirit and scope of the invention. The diameter of the third focus electrode 250 is preferably at least fifteen times greater than the diameter of the first electrode 232. The focus electrode 250 can also be made of a screen or a mesh.


The second electrode 242 has an opening 246. The opening 246 is preferably circular in this embodiment. It is within the scope of the present invention that the opening 246 can comprise other shapes such as, but not limited to, rectangular, hexagonal or octagonal. The second electrode 242 has a collar 247 (see FIG. 9B) surrounding the opening 246. The collar 247 attracts the dust contained within the airstream passing through the opening 246. As seen in the FIGS. 9B and 9C the collar 247 includes a downstream extending tubular portion 248 which can collect particles. As a result, the airstream emitted by the electrode assembly 220 has a reduced dust content.


Other similar pin-ring embodiments are shown in FIGS. 9B-9C. For example, the first electrode 232 can comprise a rod-shaped electrode having a tapered end. In FIG. 9B, a detailed cross-sectional view of the central portion of the second electrode 242 in FIG. 9A is shown. Preferably, the collar 247 is positioned in relation to the first electrode 232, such that the ionization paths from the distal tip of the first electrode 232 to the collar 247 have substantially equal path lengths. Thus, while the distal tip (or emitting tip) of the first electrode 232 is advantageously small to concentrate the electric field, the adjacent regions of the second electrode 242 preferably provide many equidistant inter-electrode paths. The lines drawn in phantom in FIGS. 9B and 9C depict theoretical electric force field lines emanating from the first electrode 232 and terminating on the curved surface of the second electrode 242. Preferably, the bulk of the field emanates within about 45 degrees of coaxial axis between the first electrode 232 and the second electrode 242.


In FIG. 9C, one or more first electrodes 232 are replaced by a conductive block 232″ of carbon fibers, the block having a distal surface in which projecting fibers 233-1, . . . 233-N take on the appearance of a “bed of nails.” The projecting fibers can each act as an emitter electrode and provide a plurality of emitting surfaces. Over a period of time, some or all of the electrodes will literally be consumed, where upon the block 232″ may be replaced. Materials other than graphite may be used for block 232″ providing that the material has a surface with projecting conductive fibers such as 233-N.


Electrode Assembly with a Downstream Trailing Electrode:



FIGS. 10A-10D



FIGS. 10A-100 illustrate an electrode assembly 220 having an array of trailing electrodes 245 added to an electrode assembly 220 similar to that shown in FIG. 7A. It is understood that an alternative embodiment similar to FIG. 10A can include a trailing electrode or electrodes without any focus electrodes and be within the spirit and scope of the inventions. Referring now to FIGS. 10A-10B, each trailing electrode 245 is located downstream of the second array of electrodes 240. Preferably, the trailing electrodes are located downstream from the second electrodes 242 by at least three times the radius R2 (see FIG. 10B). Further, the trailing electrodes 245 are preferably directly downstream of each second electrode 242 so as not to interfere with the flow of air. Also, the trailing electrode 245 is aerodynamically smooth, for example, circular, elliptical, or teardrops shaped in cross-section so as not to unduly interfere with the smoothness of the airflow thereby. In a preferred embodiment, the trailing electrodes 245 are electrically connected to the same outlet of the high voltage generator 170 as the second array of electrodes 240. As shown in FIG. 10A, the second electrodes 242 and the trailing electrodes 245 have a negative electrical charge. This arrangement can introduce more negative charges into the air stream. Alternatively, the trailing electrodes 245 can have a floating potential if they are not electrically connected. The trailing electrodes 245 can also be grounded in other embodiments. Further alternatively, as shown in FIG. 10D, the trailing electrode 245 can be formed with the second electrode out of a sheet of metal formed in the shape of the second electrode and then extending to the position of the trailing electrode and formed as a hollow trailing electrode with a peripheral wall that is about the shape of the outer surface of the trailing electrode 245 depicted in FIG. 10C.


When the trailing electrodes 245 are electrically connected to the high voltage generator 170, the positively charged particles within the airflow are also attracted to and collect on, the trailing electrodes. In a typical electrode assembly with no trailing electrode 245, most of the particles will collect on the surface area of the second electrodes 242. However, some particles will pass through the unit 200 without being collected by the second electrodes 242. Thus, the trailing electrodes 245 serve as a second surface area to collect the positively charged particles. The trailing electrodes 245 also can deflect charged particles toward the second electrodes.


The trailing electrodes 245 preferably also emit a small amount of negative ions into the airflow. These negative ions will neutralize the positive ions emitted by the first electrodes 232. If the positive ions emitted by the first electrodes 232 are not neutralized before the airflow reaches the outlet 260, the outlet fins 212 can become electrically charged and particles within the airflow may tend to stick to the fins 212. If this occurs, eventually the amount of particles collected by the fins 212 will block or minimize the airflow exiting the unit 200.



FIG. 10C illustrates another embodiment of the electrode assembly 200, having trailing electrodes 245 added to an embodiment similar to that shown in FIG. 7C. The trailing electrodes 245 are located downstream of the second array 240 similar to the previously described embodiments above. It is within the scope of the present invention to electrically connect the trailing electrodes 245 to the high voltage generator 170. As shown in FIG. 10C, all of the third focus electrodes 224 are electrically connected to the high voltage generator 170. In a preferred embodiment, only the third focus electrodes 224a1, 224b1 are electrically connected to the high voltage generator 170. The third focus electrodes 224a2, 224b2 have a floating potential.


Electrode Assemblies with Various Combinations of Focus Electrodes, Trailing Electrodes and Enhanced Second Electrodes with Protective Ends:



FIGS. 11A-11D



FIG. 11A illustrates an electrode assembly 220 that includes a first array of electrodes 230 having two wire-shaped electrodes 232-1, 232-2 (generally referred to as “electrode 232”) and a second array of electrodes 240 having three “U”-shaped electrodes 242-1, 242-2, 242-3 (generally referred to as “electrode 242”). This configuration is in contrast to, for example, the configurations of FIG. 9A, wherein there are three first emitter electrodes 232 and four second collector electrodes 242.


Upstream from each first electrode 232, at a distance X2, is a third focus electrode 224. Each third focus electrode 224a, 224b is at an angle with respect to a first electrode 232. For example, the third focus electrode 224a is preferably along a line extending from the middle of the nose 246 of the second electrode 242-2 through the center of the first electrode 232-1, as shown by extension line A. The third focus electrode 224a is in-line and symmetrically aligned with the first electrode 232-1 along extension line A. Similarly, the third focus electrode 224b is located along a line extending from middle of the nose 246 of the second electrode 242-2 through the center of the first electrode 232-2, as shown by extension line B. The third focus electrode 224b is in-line and symmetrically aligned with the first electrode 232-2 along extension line B. As previously described, the diameter of each third focus electrode 224 is preferably at least fifteen times greater than the diameter of the first electrode 232.


As shown in FIG. 11A, and similar to the embodiment shown in FIG. 5B, each second electrode preferably has a protective end 241. In a preferred embodiment, the third focus electrodes 224 are electrically connected to the high voltage generator 170 (not shown). It is within the spirit and scope of the invention to not electrically connect the third focus electrodes 224.



FIG. 11B illustrates that multiple third focus electrodes 224 may be located upstream of each first emitter electrode 232. For example, the third focus electrode 224a2 is in-line and symmetrically aligned with the third focus electrode 224a1 along extension line A. Similarly, the third focus electrode 224b2 is in-line and symmetrically aligned with the third focus electrode 242b1 along extension line B. It is within the scope of the present invention to electrically connect all, or none of the third focus electrodes 224 to the high-voltage generator 170. In a preferred embodiment, only the third focus electrodes 224a1, 224b1 are electrically connected to the high voltage generator 170, with the third focus electrodes 224a2, 224b2 having a floating potential.



FIG. 11C illustrates that the electrode assembly 220 shown in FIG. 11A may also include a trailing electrode 245 downstream of each second electrode 242. Each trailing electrode 245 is in-line with the second electrode so as not to interfere with airflow past the second electrode 242. Each trailing electrode 245 is preferably located a distance downstream of each second electrode 242 equal to at least three times the width W of the second electrode 242. It is within the scope of the present invention for the trailing electrode to by located at other distances downstream. The diameter of the trailing anode 245 is preferably no greater than the width W of the second electrode 242 to limit the interference of the airflow coming off the second electrode 242.


One aspect of the trailing electrode 245 is to direct the air trailing off the second electrode 242 and provide a more laminar flow of air exiting the outlet 260. Another aspect of the trailing electrode 245 is to neutralize the positive ions generated by the first array 230 and collect particles within the airflow. As shown in FIG. 11C, each trailing electrode 245 is electrically connected to a second electrode 242 by a conductor 248. Thus, the trailing electrode 245 is negatively charged, and serves as a collecting surface, similar to the second electrode 242, attracts the positively charged particles in the airflow. As previously described, the electrically connected trailing electrode 245 also emits negative ions to neutralize the positive ions emitted by the first electrodes 232.



FIG. 11D illustrates that a pair of third focus electrodes 224 may be located upstream of each first electrode 232. For example, the third focus electrode 224a2 is upstream of the third focus electrode 224a1 so that the third focus electrodes 224a1, 224a2 are in-line and symmetrically aligned with each other along extension line A. Similarly, the third focus electrode 224b2 is in line and symmetrically aligned with the third focus electrode 224b1 along extension line B. As previously described, preferably only the third focus electrodes 224a1, 224b1 are electrically connected to the high voltage generator 170, while the third focus electrodes 224a2, 224b2 have a floating potential. It is within the spirit and scope of the present invention to electrically connect all, or none, of the third focus electrodes to the high voltage generator 170.


Electrode Assemblies with Second Collector Electrodes Having Interstitial Electrodes:



FIGS. 11E-11F



FIG. 11E illustrates another embodiment of the electrode assembly 220 with an interstitial electrode 246. In this embodiment, the interstitial electrode 246 is located midway between the second electrodes 242. For example, the interstitial electrode 246a is located midway between the second electrodes 242-1, 242-2, while the interstitial electrode 246b is located midway between second electrodes 242-2, 242-3. Preferably, the interstitial electrode 246a, 246b are electrically connected to the first electrodes 232, and generate an electrical field with the same positive or negative charge as the first electrodes 232. The interstitial electrode 246 and the first electrode 232 then have the same polarity. Accordingly, particles traveling toward the interstitial electrode 246 will be repelled by the interstitial electrode 246 towards the second electrodes 242. Alternatively, the interstitial electrodes can have a floating potential or be grounded.


It is to be understood that interstitial electrodes 246a, 246b may also be closer to one second collector electrode than to the other. Also, the interstitial electrodes 246a, 246b are preferably located substantially near or at the protective end 241 or ends of the trailing sides 244, as depicted in FIG. 11E. Still further the interstitial electrode can be substantially located along a line between the two trailing portions or ends of the second electrodes. These rear positions are preferred as the interstitial electrodes can cause the positively charged particle to deflect towards the trailing sides 244 along the entire length of the negatively charged second collector electrode 242, in order for the second collector electrode 242 to collect more particles from the airflow.


Still further, the interstitial electrodes 246a, 246b can be located upstream along the trailing side 244 of the second collector electrodes 244. However, the closer the interstitial electrodes 246a, 246b get to the nose 246 of the second electrode 242, generally the less effective interstitial electrodes 246a, 246b are in urging positively charged particles toward the entire length the second electrodes 242. Preferably, the interstitial electrodes 246a, 246b are wire-shaped and smaller or substantially smaller in diameter than the width “W” of the second collector electrodes 242. For example, the interstitial electrodes can have a diameter of, the same as, or on the order, of the diameter of the first electrodes. For example, the interstitial electrodes can have a diameter of one-sixteenth of an inch. Also, the diameter of the interstitial electrodes 246a, 246b is substantially less than the distance between second collector electrodes, as indicated by Y2. Further the interstitial electrode can have a length or diameter in the downstream direction that is substantially less than the length of the second electrode in the downstream direction. The reason for this size of the interstitial electrodes 246a, 246b is so that the interstitial electrodes 246a, 246b have a minimal effect on the airflow rate exiting the device 100 or 200.



FIG. 11F illustrates that the electrode assembly 220 in FIG. 11E can include a pair of third electrodes 224 upstream of each first electrode 232. As previously described, the pair of third electrodes 224 are preferably in-line and symmetrically aligned with each other. For example, the third electrode 224a2 is in-line and symmetrically aligned with the third electrode 224a1 along extension line A. Extension line A preferably extends from the middle of the nose 246 of the second electrode 242-2 through the center of the first electrode 232-1. As previously disclosed, in a preferred embodiment, only the third electrodes 224a1, 224b1 are electrically connected to the high voltage generator 170. In FIG. 11F, a plurality of interstitial electrode 296a and 246b are located between the second electrodes 242. Preferably these interstitial electrodes are in-line and have a potential gradient with an increasing voltage potential on each successive interstitial electrode in the downstream direction in order to urge particles toward the second electrodes. In this situation the voltage on the interstitial electrodes would have the same sign as the voltage of the first electrode 232.


Electrode Assembly with an Enhanced First Emitter Electrode being Slack:



FIGS. 12A-12C


The previously described embodiments of the electrode assembly 220 include a first array of electrodes 230 having at least one wire-shaped electrode 232. It is within the scope of the present invention for the first array of electrodes 230 to contain electrodes consisting of other shapes and configurations.



FIG. 12A illustrates that the first array of electrodes 230 may include curved wire-shaped electrodes 252. The curved wire-shaped electrode 252 is an ion emitting surface and generates an electric field similar to the previously described wire-shaped electrodes 232. Also similar to previous embodiments, each second electrode 242 is “downstream,” and each third focus electrode 224 is “upstream,” to the curved wire-shaped electrodes 252. The electrical properties and characteristics of the second electrode 242 and the third focus electrode 224 are similar to the previously described embodiment shown in FIG. 5A. It is to be understood that an alternative embodiment of FIG. 12A can exclude the focus electrodes and be within the spirit and scope of the invention.


As shown in FIG. 12A, positive ions are generated and emitted by the first electrode 252. In general, the quantity of negative ions generated and emitted by the first electrode is proportional to the surface area of the first electrode. The height Z1 of the first electrode 252 is equal to the height Z1 of the previously disclosed wire-shaped electrode 232. However, the total length of the electrode 252 is greater than the total length of the electrode 232. By way of example only, and in a preferred embodiment, if the electrode 252 was straightened out the curved or slack wire electrode 252 is 15-30% longer than a rod or wire-shaped electrode 232. The electrode 252 is allowed to be slack to achieve the shorter height Z1. When a wire is held slack, the wire may form a curved shape similar to the first electrode 252 shown in FIG. 12A. The greater total length of the electrode 252 translates to a larger surface area than the wire-shaped electrode 232. Thus, the electrode 252 will generate and emit more ions than the electrode 232. Ions emitted by the first electrode array attach to the particulate matter within the airflow. The charged particulate matter is attracted to, and collected by, the oppositely charged second collector electrodes 242. Since the electrodes 252 generate and emit more ions than the previously described electrodes 232, more particulate matter will be removed from the airflow.



FIG. 12B illustrates that the first array of electrodes 230 may include flat coil wire-shaped electrodes 254. Each flat coil wire-shaped electrode 254 also has a larger surface area than the previously disclosed wire-shaped electrode 232. By way of example only, if the electrode 254 was straightened out, the electrode 254 will have a total length that is preferably 10% longer than the electrode 232. Since the height of the electrode 254 remains at Z1, the electrode 254 has a “kinked” configuration as shown in FIG. 12B. This greater length translates to a larger surface area of the electrode 254 than the surface area of the electrode 232. Accordingly, the electrode 254 will generate and emit a greater number of ions than electrode 232. It is to be understood that an alternative embodiment of FIG. 12B can exclude the focus electrodes and be within the spirit and scope of the invention.



FIG. 12C illustrates that the first array of electrodes 230 may also include coiled wire-shaped electrodes 256. Again, the height Z1 of the electrodes 256 is similar to the height Z1 of the previously described electrodes 232. However, the total length of the electrodes 256 is greater than the total length of the electrodes 232. In a preferred embodiment, if the coiled electrode 256 was straightened out the electrodes 256 will have a total length two to three times longer than the wire-shaped electrodes 232. Thus, the electrodes 256 have a larger surface area than the electrodes 232, and generate and emit more ions than the first electrodes 232. The diameter of the wire that is coiled to produce the electrode 256 is similar to the diameter of the electrode 232. The diameter of the electrode 256 itself is preferably 1-3 mm, but can be smaller in accordance with the diameter of first emitter electrode 232. The diameter of the electrode 256 shall remain small enough so that the electrode 256 has a high emissivity and is an ion emitting surface. It is to be understood that an alternative embodiment of FIG. 12C can exclude the focus electrodes and be within the spirit and scope of the invention.


The electrodes 252, 254 and 256 shown in FIGS. 12A-12C may be incorporated into any of the electrode assembly 220 configurations previously disclosed in this application.


Turning now to FIG. 13A, a first embodiment of an electrode cleaning mechanism 500 is depicted. In the embodiment shown, mechanism 500 comprises a flexible sheet of insulating material such as MYLAR or other high voltage, high temperature breakdown resistant material, having sheet thickness of perhaps 0.1 mm or so. Sheet 500 is attached at one end to the base or other mechanism 113 secured to the lower end of second electrode array 240. Sheet 500 extends or projects out from base 113 towards and beyond the location of first electrode array 230 electrodes 232. The overall projection length of sheet 500 in FIG. 13A will be sufficiently long to span the distance between base 113 of the second array 240 and the location of electrodes 232 in the first array 230. This span distance will depend upon the electrode array configuration but typically will be a few inches or so. Preferably the distal edge of sheet 500 will extend slightly beyond the location of electrodes 232, perhaps 0.5″ beyond. As shown in FIGS. 13A and 13C, the distal edge, e.g., edge closest to electrodes 232, of material 500 is formed with a slot 510 corresponding to the location of an electrode 232. Preferably the inward end of the slot forms a small circle 520, which can promote flexibility.


The configuration of material 500 and slots 510 is such that each wire or wire-like electrode 232 in the first electrode array 230 fits snugly and frictionally within a corresponding slot 510. As indicated by FIG. 13A and shown in FIG. 13C, instead of a single sheet 500 that includes a plurality of slots 510, instead one can provide individual strips 515 of material 500, the distal end of each strip having a slot 510 that will surround an associated wire electrode 232. Note in FIGS. 13B and 13C that sheet 500 or sheets 515 may be formed with holes 119 that can attach to pegs 117 that project from the base portion 113 of the second electrode array 240. Of course other attachment mechanisms could be used including glue, double-sided tape, inserting the array 240-facing edge of the sheet into a horizontal slot or ledge in base member 113, and so forth.



FIG. 13A shows second electrode array 240 in the process of being moved upward, perhaps by a user intending to remove array 240 to remove particulate matter from the surfaces of its electrodes 242. Note that as array 240 moves up (or down), sheet 510 (or sheets 515) also move up (or down). This vertical movement of array 240 produces a vertical movement in sheet 510 or 515, which causes the outer surface of electrodes 232 to scrape against the inner surfaces of an associated slot 510. FIG. 13A, for example, shows debris and other deposits 612 (indicated by x's) on wires 232 above sheet 500. As array 240 and sheet 500 move upward, debris 612 is scraped off the wire electrodes, and falls downward (to be vaporized or collected as particulate matter when unit 100 is again reassembled and turned-on). Thus, the outer surface of electrodes 232 below sheet 500 in FIG. 13A is shown as being cleaner than the surface of the same electrodes above sheet 500, where scraping action has yet to occur.


A user hearing that excess noise or humming emanates from unit 100 might simply turn the unit off, and slide array 240 (and thus sheet 500 or sheets 515) up and down (as indicated by the up/down arrows in FIG. 13A) to scrape the wire electrodes in the first electrode array. This technique does not damage the wire electrodes, and allows the user to clean as required.


As noted earlier, a user may remove second electrode array 240 for cleaning (thus also removing sheet 500, which will have scraped electrodes 232 on its upward vertical path). If the user cleans electrodes 242 with water and returns array 240 to unit 100 without first completely drying 240, moisture might form on the upper surface of a horizontally disposed member 550 within unit 100. Thus, as shown in FIG. 13B, it is preferred that an upwardly projecting vane 560 be disposed near the base of each electrode 232 such that when array 240 is fully inserted into unit 100, the distal portion of sheet 500 or preferably sheet strips 515 deflect upward. While sheet 500 or sheets 515 nominally will define an angle θ of about 90 degrees, as base 113 becomes fully inserted into unit 100, the angle θ will increase, approaching 0 degrees, e.g., the sheet is extending almost vertically upward. If desired, a portion of sheet 500 or sheet strips 515 can be made stiffer by laminating two or more layers of MYLAR or other material. For example the distal tip of strip 515 in FIG. 13B might be one layer thick, whereas the half or so of the strip length nearest electrode 242 might be stiffened with an extra layer or two of Mylar or similar material.


The inclusion of a projecting vane 560 in the configuration of FIG. 13B advantageously disrupted physical contact between sheet 500 or sheet strips 515 and electrodes 232, thus tending to preserve a high ohmic impedance between the first and second electrode arrays 230, 240. The embodiment of FIGS. 14A-14D advantageously serves to pivot sheet 500 or sheet strips 515 upward, essentially parallel to electrodes 232, to help maintain a high impedance between the first and second electrode arrays. Note the creation of an air gap 513 resulting from the upward deflection of the slit distal tip of strip 515 in FIG. 13B.


In FIG. 14A, the lower edges of second array electrodes 242 are retained by a base member 113 from which project arms 677, which can pivot about pivot axle 687. Preferably axle 687 biases arms 677 into a horizontal disposition, e.g., such that θ approximately equals 90 degrees. Arms 645 project from the longitudinal axis of base member 113 to help member 113 align itself within an opening 655 formed in member 550, described below. Preferably base member 113 and arms 677 are formed from a material that exhibits high voltage breakdown and can withstand high temperature. Ceramic is a preferred material (if cost and weight were not considered), but certain plastics could also be used. The unattached tip of each arm 677 terminates in a sheet strip 515 of MYLAR, KAPTON, or a similar material, whose distal tip terminates in a slot 510. It is seen that the pivotable arms 677 and sheet strips 515 are disposed such that each slot 510 will self-align with a wire or wire-like electrode 232 in first array 230. Electrodes 232 preferably extend from pylons 627 on a base member 550 that extends from legs 565 from the internal bottom of the housing of the transporter-conditioner unit. To further help maintain high impedance between the first and second electrode arrays, base member 550 preferably includes a barrier wall 665 and upwardly extending vanes 675. Vanes 675, pylons 627, and barrier wall 665 extend upward perhaps an inch or so, depending upon the configuration of the two electrode be formed integrally, e.g., by casting, from a material that exhibits high voltage breakdown and can withstand high temperature, ceramic, or certain plastics for example.


As best seen in FIG. 14A, base member 550 includes an opening 655 sized to receive the lower portion of second electrode array base member 113. In FIGS. 14A and 14B, arms 677 and sheet material 515 are shown pivoting from base member 113 about axis 687 at an angle θ approximately equal 90 degrees. In this disposition, an electrode 232 will be within the slot 510 formed at the distal tip of each sheet material member 515.


Assume that a user had removed second electrode array 240 completely from the transporter-conditioner unit for cleaning, and that FIGS. 14A and 14B depict array 240 being reinserted into the unit. The coiled spring or other bias mechanism associated with pivot axle 687 will urge arms 677 into an angle θ approximately equal 90 degrees. orientation as the user inserts array 240 into unit 100. Side projections 645 help base member 113 align properly such that each wire or wire-like electrode 232 is caught within the slot 510 of a member 515 on an arm 677. As the user slides array 240 down into unit 100, there will be a scraping action between the portions of sheet member 515 on either side of a slot 510, and the outer surface of an electrode 232 that is essentially captured within the slot. This friction will help remove debris or deposits that may have formed on the surface of electrodes 232. The user may slide array 240 up and down the further promote the removal of debris or deposits from elements 232.


In FIG. 14C the user has slid array 240 down almost entirely into unit 100. In the embodiment shown, when the lowest portion of base member 232 is perhaps an inch or so above the planar surface of member 550, the upward edge of a vane 675 will strike the a lower surface region of a projection arm 677. The result will be to pivot arm 677 and the attached slit-member 515 about axle 687 such that the angle θ decreases. In the disposition shown in FIG. 14C, θ approximately equals 45 degrees and slit-contact with an associated electrode 232 is no longer made.


In FIG. 14D, the user has firmly urged array 240 fully downward into transporter-conditioner unit 100. In this disposition, as the projecting bottommost portion of member 113 begins to enter opening 655 in member 550 (see FIG. 14A), contact between the inner wall 657 portion of member 550 urges each arm 677 to pivot fully upward, e.g., θ approximately equals 0 degrees. Thus in the fully inserted disposition shown in FIG. 14D, each slit electrode cleaning member 515 is rotated upward parallel to its associated electrode 232. As such, neither arm 677 nor member 515 will decrease impedance between first and second electrode arrays 230, 240. Further, the presence of vanes 675 and barrier wall 665 further promote high impedance.


Thus, the embodiments shown in FIGS. 13A-14D depict alternative configurations for a cleaning mechanism for a wire or wire-like electrode in a transporter-conditioner unit.


Turning now to FIGS. 15A-15E, various bead-like mechanisms are shown for cleaning deposits from the outer surface of wire electrodes 232 in a first electrode array 230 in a transporter-converter unit. In FIG. 15A a symmetrical bead 600 is shown surrounding wire element 232, which is passed through bead channel 610 at the time the first electrode array is fabricated. Bead 600 is fabricated from a material that can withstand high temperature and high voltage, and is not likely to char, ceramic or glass, for example. While a metal bead would also work, an electrically conductive bead material would tend slightly to decrease the resistance path separating the first and second electrode arrays, e.g., by approximately the radius of the metal bead. In FIG. 15A, debris and deposits 612 on electrode 232 are depicted as “x's”. In FIG. 15A, bead 600 is moving in the direction shown by the arrow relative to wire 232. Such movement can result from the user inverting unit 100, e.g., turning the unit upside down. As bead 600 slides in the direction of the arrow, debris and deposits 612 scrape against the interior walls of channel 610 and are removed. The removed debris can eventually collect at the bottom interior of the transporter-conditioner unit. Such debris will be broken down and vaporized as the unit is used, or will accumulate as particulate matter on the surface of electrodes 242. If wire 232 has a nominal diameter of say 0.1 mm, the diameter of bead channel 610 will be several times larger, perhaps 0.8 mm or so, although greater or lesser size tolerances may be used. Bead 600 need not be circular and may instead be cylindrical as shown by bead 600′ in FIG. 15A. A circular bead may have a diameter in the range of perhaps 0.3″ to perhaps 0.5″. A cylindrical bead might have a diameter of say 0.3″ and be about 0.5″ tall, although different sizes could of course be used.


As indicated by FIG. 15A, an electrode 232 may be strung through more than one bead 600, 600′. Further, as shown by FIGS. 15B-15D, beads having different channel symmetries and orientations may be used as well. It is to be noted that while it may be most convenient to form channels 610 with circular cross-sections, the cross-sections could in fact be non-circular, e.g., triangular, square, irregular shape, etc.



FIG. 15B shows a bead 600 similar to that of FIG. 15A, but wherein channel 610 is formed off-center to give asymmetry to the bead. An off-center channel will have a mechanical moment and will tend to slightly tension wire electrode 232 as the bead slides up or down, and can improve cleaning characteristics. For ease of illustration, FIGS. 15B-15E do not depict debris or deposits on or removed from wire or wire-like electrode 232. In the embodiment of FIG. 15C, bead channel 610 is substantially in the center of bead 600 but is inclined slightly, again to impart a different frictional cleaning action. In the embodiment of FIG. 15D, beam 600 has a channel 610 that is both off center and inclined, again to impart a different frictional cleaning action. In general, asymmetrical bead channel or through-opening orientations are preferred.



FIG. 15E depicts an embodiment in which a bell-shaped walled bead 620 is shaped and sized to fit over a pillar 550 connected to a horizontal portion 560 of an interior bottom portion of unit 100. Pillar 550 retains the lower end of wire or wire-like electrode 232, which passes through a channel 630 in bead 620, and if desired, also through a channel 610 in another bead 600. Bead 600 is shown in phantom in FIG. 15E to indicate that it is optional.


Friction between debris 612 on electrode 232 and the mouth of channel 630 will tend to remove the debris from the electrode as bead 620 slides up and down the length of the electrode, e.g., when a user inverts transporter-conditioner unit 100, to clean electrodes 232. It is understood that each electrode 232 will include its own bead or beads, and some of the beads may have symmetrically disposed channels, while other beads may have asymmetrically disposed channels. An advantage of the configuration shown in FIG. 15E is that when unit 100 is in use, e.g., when bead 620 surrounds pillar 550, with an air gap therebetween, improved breakdown resistance is provided, especially when bead 620 is fabricated from glass or ceramic or other high voltage, high temperature breakdown material that will not readily char. The presence of an air gap between the outer surface of pillar 550 and the inner surface of the bellshaped bead 620 helps increase this resistance to high voltage breakdown or arcing, and to charring.


The foregoing description of the preferred embodiments of the present invention has been provided for the purposes of illustration and description. It is not intended to be exhaustive or to limit the invention to the precise forms disclosed. Many modifications and variations will be apparent to the practitioner skilled in the art. Modifications and variations may be made to the disclosed embodiments without departing from the subject and spirit of the invention as defined by the following claims. Embodiments were chosen and described in order to best describe the principles of the invention and its practical application, thereby enabling others skilled in the art to understand the invention, the various embodiments and with various modifications that are suited to the particular use contemplated. It is intended that the scope of the invention be defined by the following claims and their equivalents.

Claims
  • 1. An apparatus comprising: an elongated electrode energizable with respect to at least one other electrode to generate ions and to thereby electro-kinetically motivate airflow between an intake and an exhaust outflow of the apparatus; anda cleaning device positioned to frictionally engage at least two opposing surfaces of the elongated electrode, and to define a mechanical moment imparting channel through which the elongated electrode passes, thereby tensioning the elongated electrode in connection with movement of the cleaning device along a length of the elongated electrode to remove debris or deposits from the at least two opposing surfaces of the elongated electrode.
  • 2. The apparatus of claim 1, wherein the mechanical moment imparting channel is arranged to partially bind upon the elongated electrode during movement of the cleaning device.
  • 3. The apparatus of claim 1, wherein the mechanical moment imparting channel defined by the cleaning device is inclined relative to the elongate extent of the elongated electrode to impart the tension to the elongated electrode as the cleaning device moves along the elongated electrode.
  • 4. The apparatus of claim 1, wherein the cleaning device comprises a flexible member defining a slot for receiving the elongated electrode and for frictionally engaging the two opposing surfaces of the elongated electrode.
  • 5. The apparatus of claim 1, wherein the mechanical moment imparting channel includes a through-bore of a bead, wherein the through-bore is formed off-center, inclined or both off-center and inclined to provide the tensioning of the elongated electrode and the frictionally engaging with the two opposing surfaces of the elongated electrode.
  • 6. The apparatus of claim 1, wherein the cleaning device is moveable in response to movement of the other electrode.
  • 7. The apparatus of claim 1, wherein the cleaning device is moveable in response to a change in orientation of the apparatus.
  • 8. The apparatus of claim 1, wherein the cleaning device is moveable by a manual operation.
  • 9. The apparatus of claim 1, wherein the mechanical moment imparting channel is provided using a bead that, in cross-section, substantially surrounds the elongated electrode.
  • 10. The apparatus of claim 1, wherein surfaces of the mechanical moment imparting channel that frictionally engage the elongated electrode are fabricated of at least one of ceramic and glass.
  • 11. The apparatus of claim 1, wherein the cleaning device defines a slot extending from an edge of the device with the elongated electrode received in the slot.
  • 12. The apparatus of claim 11, wherein the slot is tapered to provide increased frictional engagement with the elongated electrode at increased depths within the slot.
  • 13. The apparatus of claim 1, wherein a body of the cleaning device is asymmetrical relative to the elongated electrode such that the mechanical moment imparting channel of the cleaning device acts on the elongated electrode substantially orthogonal to a longitudinal axis of the elongated electrode.
  • 14. The apparatus of claim 1, wherein the mechanical moment imparting channel of the cleaning device is substantially off-center relative to the elongated electrode to frictionally bind upon the elongated electrode during movement of the cleaning device.
  • 15. The apparatus of claim 14, wherein the mechanical moment imparting channel of the cleaning device is further inclined relative to the elongated electrode to frictionally bind upon the elongated electrode during movement of the cleaning device.
  • 16. The apparatus of claim 1, wherein the elongated electrode is one of an emitter electrode and a collector electrode.
  • 17. The apparatus of claim 1, further comprising the other electrode and wherein the other electrode is one of an emitter electrode and a collector electrode.
  • 18. The apparatus of claim 1, wherein the mechanical moment imparting channel material in frictional engagement with the elongated electrode is electrically conductive.
  • 19. The apparatus of claim 1, wherein the mechanical moment imparting channel material in frictional engagement with the elongated electrode is a glass or ceramic.
  • 20. A method comprising: in an electro-kinetic air mover system, energizing an elongated electrode with respect to at least one other electrode to generate ions and to thereby electro-kinetically motivate airflow between an intake and an exhaust outflow; andmoving a cleaning device along a length of the elongated electrode and in frictional engagement with at least two opposing surfaces of the elongated electrode, the cleaning device defining a mechanical moment imparting channel through which the elongated electrode passes and which thereby tensions the elongated electrode; andby the frictionally engaged movement of the cleaning device along a length of the elongated electrode removing debris or deposits accumulated, during energized operation of the electro-kinetic air mover system, on the elongated electrode.
  • 21. The method of claim 20, further comprising: elastically deforming the elongated electrode in the mechanical moment imparting channel in a direction substantially orthogonal a longitudinal axis of the elongated electrode.
  • 22. The method of claim 20, wherein the mechanical moment imparting channel is arranged to partially bind upon the elongated electrode as the cleaning device is moved therealong.
  • 23. The method of claim 20, wherein the mechanical moment imparting channel is inclined relative to the elongate extent of the elongated electrode to impart the tension to the elongated electrode as the cleaning device is moved therealong.
  • 24. The method of claim 20, wherein the mechanical moment imparting channel material in frictional engagement with the elongated electrode is electrically conductive.
  • 25. The method of claim 20, wherein the mechanical moment imparting channel material in frictional engagement with the elongated electrode is a glass or ceramic.
CROSS-REFERENCE TO RELATED APPLICATION(S)

This application is a continuation of application Ser. No. 12/723,102, filed Mar. 12, 2010, now U.S. Pat. No. 7,976,615, which in turn is a continuation of application Ser. No. 10/074,209, filed Feb. 12, 2002, now U.S. Pat. No. 7,695,690 which in turn claims benefit of provisional Application No. 60/341,090, filed Dec. 13, 2001 and provisional Application No. 60/306,479, filed Jul. 18, 2001. application Ser. No. 10/074,209, now U.S. Pat. No. 7,695,690 is also a continuation-in part of application Ser. No. 09/730,499, filed Dec. 5, 2000, now U.S. Pat. No. 6,713,026, which itself is a continuation of application Ser. No. 09/186,471, filed Nov. 5, 1998, now U.S. Pat. No. 6,176,977. application Ser. No. 10/074,209, now U.S. Pat. No. 7,695,690 is also a continuation-in-part of application Ser. No. 09/924,624, filed Aug. 8, 2001, now abandoned, which itself is a continuation of application Ser. No. 09/564,960, filed May 4, 2000, now U.S. Pat. No. 6,350,417 which itself is a continuation-in-part of application Ser. No. 09/186,471, filed Nov. 5, 1998, now U.S. Pat. No. 6,176,977. Each of the aforementioned applications (including the provisional applications) is incorporated herein by reference. This application is related to the following patent applications: U.S. patentapplication No.FiledU.S. Pat. No.90/007,276Oct. 29, 20046,504,308 C111/041,926Jan. 21, 2005RE41,81211/091,243Mar. 28, 20057,285,15511/062,057Feb. 18, 200511/071,779Mar. 3, 20057,767,16510/994,869Nov. 22, 20047,767,16911/007,556Dec. 8, 20047,291,20710/074,209Feb. 12, 20027,695,69010/685,182Oct. 14, 20037,404,93510/944,016Sep. 17, 200410/795,934Mar. 8, 20047,517,50410/435,289May 9, 200311/064,797Feb. 24, 200511/003,671Dec. 3, 200411/003,035Dec. 3, 20047,318,85611/007,395Dec. 8, 20047,897,11810/876,495Jun. 25, 200410/809,923Mar. 25, 20047,405,67211/004,397Dec. 3, 200410/895,799Jul. 21, 200410/642,927Aug. 18, 200311/823,346Apr. 12, 200410/662,591Sep. 15, 20037,371,35411/061,967Feb. 18, 200511/150,046Jun. 10, 20057,662,34811/188,448Jul. 25, 200511/188,478Jul. 25, 20057,311,76211/293,538Dec. 2, 20057,892,50111/457,396Jul. 13, 200611/464,139Aug. 11, 200611/694,281Mar. 30, 2007 The following applications are incorporated by reference: U.S. patentapplication No.FiledU.S. Pat. No.60/341,518Dec. 13, 200160/341,433Dec. 13, 200160/341,592Dec. 13, 200160/341,320Dec. 13, 200160/341,179Dec. 13, 200160/340,702Dec. 13, 200160/341,377Dec. 13, 200110/023,197Dec. 13, 200110/023,460Dec. 13, 200160/340,288Dec. 13, 200160/341,176Dec. 13, 200160/340,462Dec. 13, 200110/074,082Feb. 12, 20026,958,13410/074,207Feb. 12, 200210/074,208Feb. 12, 200210/074,339Feb. 12, 200210/074,827Feb. 12, 200210/074,096Feb. 12, 20026,974,56010/074,347Feb. 12, 20026,911,18610/074,379Feb. 12, 200210/074,549Feb. 12, 200210/074,103Feb. 12, 2002

US Referenced Citations (484)
Number Name Date Kind
653421 Lorey Jul 1900 A
895729 Carlborg Aug 1908 A
995958 Goldberg Jun 1911 A
1469275 Moller et al. Oct 1923 A
1791338 Wintermute Feb 1931 A
1869335 Day Jul 1932 A
1882949 Ruder Oct 1932 A
2129783 Penney Sep 1938 A
2247409 Roper Jul 1941 A
2327588 Bennett Aug 1943 A
2359057 Skinner Sep 1944 A
2509548 White May 1950 A
2590447 Nord et al. Mar 1952 A
2826262 Byerly Mar 1958 A
2949550 Brown Aug 1960 A
2978006 Nodolf Apr 1961 A
3018394 Brown Jan 1962 A
3026964 Penney Mar 1962 A
3374941 Okress Mar 1968 A
3412530 Cardiff Nov 1968 A
3518462 Brown Jun 1970 A
3540191 Herman Nov 1970 A
3581470 Aitkenhead et al. Jun 1971 A
3638058 Fritzius Jan 1972 A
3744216 Halloran Jul 1973 A
3806763 Masuda Apr 1974 A
3892927 Lindenberg Jul 1975 A
3945813 Iinoya et al. Mar 1976 A
3958960 Bakke May 1976 A
3958961 Bakke May 1976 A
3958962 Hayashi May 1976 A
3981695 Fuchs Sep 1976 A
3984215 Zucker Oct 1976 A
3988131 Kanazawa et al. Oct 1976 A
4007024 Sallee et al. Feb 1977 A
4052177 Kide Oct 1977 A
4056372 Hayashi Nov 1977 A
4070163 Kolb et al. Jan 1978 A
4074983 Bakke Feb 1978 A
4092134 Kikuchi May 1978 A
4097252 Kirchhoff et al. Jun 1978 A
4102654 Pellin Jul 1978 A
4104042 Brozenick Aug 1978 A
4110086 Schwab et al. Aug 1978 A
4119415 Hayashi et al. Oct 1978 A
4126434 Keiichi Nov 1978 A
4138233 Masuda Feb 1979 A
4147522 Gonas et al. Apr 1979 A
4155792 Gelhaar et al. May 1979 A
4171975 Kato et al. Oct 1979 A
4185971 Isahaya Jan 1980 A
4189308 Feldman Feb 1980 A
4205969 Matsumoto Jun 1980 A
4209306 Feldman et al. Jun 1980 A
4218225 Kirchhoff et al. Aug 1980 A
4225323 Zarchy et al. Sep 1980 A
4227894 Proynoff Oct 1980 A
4231766 Spurgin Nov 1980 A
4232355 Finger et al. Nov 1980 A
4244710 Burger Jan 1981 A
4244712 Tongret Jan 1981 A
4251234 Chang Feb 1981 A
4253852 Adams Mar 1981 A
4259093 Vlastos et al. Mar 1981 A
4259452 Yukuta et al. Mar 1981 A
4259707 Penney Mar 1981 A
4264343 Natarajan et al. Apr 1981 A
4266948 Teague et al. May 1981 A
4282014 Winkler et al. Aug 1981 A
4284420 Borysiak Aug 1981 A
4289504 Scholes Sep 1981 A
4293319 Claassen, Jr. Oct 1981 A
4308036 Zahedi et al. Dec 1981 A
4315188 Cerny et al. Feb 1982 A
4318718 Utsumi et al. Mar 1982 A
4342571 Hayashi Aug 1982 A
4357150 Masuda et al. Nov 1982 A
4386395 Francis, Jr. May 1983 A
4413225 Donig et al. Nov 1983 A
4414603 Masuda Nov 1983 A
4445911 Lind May 1984 A
4477263 Shaver et al. Oct 1984 A
4496375 Le Vantine Jan 1985 A
4502002 Ando Feb 1985 A
4509958 Masuda et al. Apr 1985 A
4514780 Brussee et al. Apr 1985 A
4515982 Lechtken et al. May 1985 A
4516991 Kawashima May 1985 A
4521229 Baker et al. Jun 1985 A
4522634 Frank Jun 1985 A
4534776 Mammel et al. Aug 1985 A
4536698 Shevalenko et al. Aug 1985 A
4544382 Taillet et al. Oct 1985 A
4555252 Eckstein Nov 1985 A
4569684 Ibbott Feb 1986 A
4582961 Frederiksen Apr 1986 A
4587475 Finney, Jr. et al. May 1986 A
4588423 Gillingham et al. May 1986 A
4590042 Drage May 1986 A
4597780 Reif Jul 1986 A
4597781 Spector Jul 1986 A
4600411 Santamaria Jul 1986 A
4601733 Ordines et al. Jul 1986 A
4604174 Bollinger et al. Aug 1986 A
4614573 Masuda Sep 1986 A
4623365 Bergman Nov 1986 A
4626261 Jorgensen Dec 1986 A
4632135 Lenting et al. Dec 1986 A
4632746 Bergman Dec 1986 A
4636981 Ogura Jan 1987 A
4643744 Brooks Feb 1987 A
4643745 Sakakibara et al. Feb 1987 A
4647836 Olsen Mar 1987 A
4650648 Beer et al. Mar 1987 A
4656010 Leitzke et al. Apr 1987 A
4657738 Kanter et al. Apr 1987 A
4659342 Lind Apr 1987 A
4662903 Yanagawa May 1987 A
4666474 Cook May 1987 A
4668479 Manabe et al. May 1987 A
4670026 Hoenig Jun 1987 A
4673416 Sakakibara et al. Jun 1987 A
4674003 Zylka Jun 1987 A
4680496 Letournel et al. Jul 1987 A
4686370 Blach Aug 1987 A
4689056 Noguchi et al. Aug 1987 A
4691829 Auer Sep 1987 A
4692174 Gelfand et al. Sep 1987 A
4693869 Pfaff Sep 1987 A
4694376 Gesslauer Sep 1987 A
4702752 Yanagawa Oct 1987 A
4713092 Kikuchi et al. Dec 1987 A
4713093 Hansson Dec 1987 A
4713724 Voelkel Dec 1987 A
4715870 Masuda et al. Dec 1987 A
4725289 Quintilian Feb 1988 A
4726812 Hirth Feb 1988 A
4726814 Weitman Feb 1988 A
4736127 Jacobsen Apr 1988 A
4743275 Flanagan May 1988 A
4749390 Burnett et al. Jun 1988 A
4750921 Sugita et al. Jun 1988 A
4760302 Jacobsen Jul 1988 A
4760303 Miyake Jul 1988 A
4765802 Gombos et al. Aug 1988 A
4771361 Varga Sep 1988 A
4772297 Anzai Sep 1988 A
4779182 Mickal et al. Oct 1988 A
4781736 Cheney et al. Nov 1988 A
4786844 Farrell et al. Nov 1988 A
4789801 Lee Dec 1988 A
4808200 Dallhammer et al. Feb 1989 A
4811159 Foster, Jr. Mar 1989 A
4822381 Mosley et al. Apr 1989 A
4853005 Jaisinghani et al. Aug 1989 A
4869736 Ivester et al. Sep 1989 A
4892713 Newman Jan 1990 A
4929139 Vorreiter et al. May 1990 A
4940470 Jaisinghani et al. Jul 1990 A
4940894 Morters Jul 1990 A
4941068 Hofmann Jul 1990 A
4941224 Saeki et al. Jul 1990 A
4944778 Yanagawa Jul 1990 A
4954320 Birmingham et al. Sep 1990 A
4955991 Torok et al. Sep 1990 A
4966666 Waltonen Oct 1990 A
4967119 Torok et al. Oct 1990 A
4976752 Torok et al. Dec 1990 A
4978372 Pick Dec 1990 A
D315598 Yamamoto et al. Mar 1991 S
5003774 Leonard Apr 1991 A
5006761 Torok et al. Apr 1991 A
5010869 Lee Apr 1991 A
5012093 Shimizu Apr 1991 A
5012094 Hamade Apr 1991 A
5012159 Torok et al. Apr 1991 A
5022979 Hijikata et al. Jun 1991 A
5024685 Torok et al. Jun 1991 A
5030254 Heyen et al. Jul 1991 A
5037456 Yu Aug 1991 A
5043033 Fyfe Aug 1991 A
5045095 You Sep 1991 A
5053912 Loreth et al. Oct 1991 A
5059219 Plaks et al. Oct 1991 A
5061462 Suzuki Oct 1991 A
5066313 Mallory, Sr. Nov 1991 A
5072746 Kantor Dec 1991 A
5076820 Gurvitz Dec 1991 A
5077468 Hamade Dec 1991 A
5077500 Torok et al. Dec 1991 A
5100440 Stahel et al. Mar 1992 A
RE33927 Fuzimura May 1992 E
D326514 Alsup et al. May 1992 S
5118942 Hamade Jun 1992 A
5125936 Johansson Jun 1992 A
5136461 Zellweger Aug 1992 A
5137546 Steinbacher et al. Aug 1992 A
5141529 Oakley et al. Aug 1992 A
5141715 Sackinger et al. Aug 1992 A
D329284 Patton Sep 1992 S
5147429 Bartholomew et al. Sep 1992 A
5154733 Fujii et al. Oct 1992 A
5158580 Chang Oct 1992 A
D332655 Lytle Jan 1993 S
5180404 Loreth et al. Jan 1993 A
5183480 Raterman et al. Feb 1993 A
5196171 Peltier Mar 1993 A
5198003 Haynes Mar 1993 A
5199257 Colletta et al. Apr 1993 A
5210678 Lain et al. May 1993 A
5215558 Moon Jun 1993 A
5217504 Johansson Jun 1993 A
5217511 Plaks et al. Jun 1993 A
5234555 Ibbott Aug 1993 A
5248324 Hara Sep 1993 A
5250267 Johnson et al. Oct 1993 A
5254155 Mensi Oct 1993 A
5266004 Tsumurai et al. Nov 1993 A
5271763 Jang Dec 1993 A
5282891 Durham Feb 1994 A
5290343 Morita et al. Mar 1994 A
5296019 Oakley et al. Mar 1994 A
5302190 Williams Apr 1994 A
5308586 Fritsche et al. May 1994 A
5315838 Thompson May 1994 A
5316741 Sewell et al. May 1994 A
5330559 Cheney et al. Jul 1994 A
5348571 Weber Sep 1994 A
5376168 Inculet Dec 1994 A
5378978 Gallo et al. Jan 1995 A
5386839 Chen Feb 1995 A
5395430 Lundgren et al. Mar 1995 A
5401301 Schulmerich et al. Mar 1995 A
5401302 Schulmerich et al. Mar 1995 A
5403383 Jaisinghani Apr 1995 A
5405434 Inculet Apr 1995 A
5407469 Sun Apr 1995 A
5407639 Watanabe et al. Apr 1995 A
5417936 Suzuki et al. May 1995 A
5419953 Chapman May 1995 A
5433772 Sikora Jul 1995 A
5435817 Davis et al. Jul 1995 A
5435978 Yokomi Jul 1995 A
5437713 Chang Aug 1995 A
5437843 Kuan Aug 1995 A
5466279 Hattori et al. Nov 1995 A
5468454 Kim Nov 1995 A
5474599 Cheney et al. Dec 1995 A
5484472 Weinberg Jan 1996 A
5484473 Bontempi Jan 1996 A
5492678 Ota et al. Feb 1996 A
5501844 Kasting, Jr. et al. Mar 1996 A
5503808 Garbutt et al. Apr 1996 A
5503809 Coate et al. Apr 1996 A
5505914 Tona-Serra Apr 1996 A
5508008 Wasser Apr 1996 A
5514345 Garbutt et al. May 1996 A
5516493 Bell et al. May 1996 A
5518531 Joannu May 1996 A
5520887 Shimizu et al. May 1996 A
5525310 Decker et al. Jun 1996 A
5529613 Yavnieli Jun 1996 A
5529760 Burris Jun 1996 A
5532798 Nakagami et al. Jul 1996 A
5535089 Ford et al. Jul 1996 A
5536477 Cha et al. Jul 1996 A
5538695 Shinjo et al. Jul 1996 A
5540761 Yamamoto Jul 1996 A
5542967 Ponizovsky et al. Aug 1996 A
5545379 Gray Aug 1996 A
5545380 Gray Aug 1996 A
5547643 Nomoto et al. Aug 1996 A
5549874 Kamiya et al. Aug 1996 A
5554344 Duarte Sep 1996 A
5554345 Kitchenman Sep 1996 A
5565685 Czako et al. Oct 1996 A
5569368 Larsky et al. Oct 1996 A
5569437 Stiehl et al. Oct 1996 A
D375546 Lee Nov 1996 S
5571483 Pfingstl et al. Nov 1996 A
5573577 Joannou Nov 1996 A
5573730 Gillum Nov 1996 A
5578112 Krause Nov 1996 A
5578280 Kazi et al. Nov 1996 A
5582632 Nohr et al. Dec 1996 A
5587131 Malkin et al. Dec 1996 A
D377523 Marvin et al. Jan 1997 S
5591253 Altman et al. Jan 1997 A
5591334 Shimizu et al. Jan 1997 A
5591412 Jones et al. Jan 1997 A
5593476 Coppom Jan 1997 A
5601636 Glucksman Feb 1997 A
5603752 Hara Feb 1997 A
5603893 Gundersen et al. Feb 1997 A
5614002 Chen Mar 1997 A
5624476 Eyraud Apr 1997 A
5630866 Gregg May 1997 A
5630990 Conrad et al. May 1997 A
5637198 Breault Jun 1997 A
5637279 Besen et al. Jun 1997 A
5641342 Smith et al. Jun 1997 A
5641461 Ferone Jun 1997 A
5647890 Yamamoto Jul 1997 A
5648049 Jones et al. Jul 1997 A
5655210 Gregoire et al. Aug 1997 A
5656063 Hsu Aug 1997 A
5665147 Taylor et al. Sep 1997 A
5667563 Silva, Jr. Sep 1997 A
5667564 Weinberg Sep 1997 A
5667565 Gondar Sep 1997 A
5667756 Ho Sep 1997 A
5669963 Horton et al. Sep 1997 A
5678237 Powell et al. Oct 1997 A
5681434 Eastlund Oct 1997 A
5681533 Hiromi Oct 1997 A
5698164 Kishioka et al. Dec 1997 A
5702507 Wang Dec 1997 A
D389567 Gudefin Jan 1998 S
5766318 Loreth et al. Jun 1998 A
5779769 Jiang Jul 1998 A
5785631 Heidecke Jul 1998 A
5814135 Weinberg Sep 1998 A
5879435 Satyapal et al. Mar 1999 A
5893977 Pucci Apr 1999 A
5911957 Khatchatrian et al. Jun 1999 A
5972076 Nichols et al. Oct 1999 A
5975090 Taylor et al. Nov 1999 A
5980614 Loreth et al. Nov 1999 A
5993521 Loreth et al. Nov 1999 A
5993738 Goswani Nov 1999 A
5997619 Knuth et al. Dec 1999 A
6019815 Satyapal et al. Feb 2000 A
6042637 Weinberg Mar 2000 A
6063168 Nichols et al. May 2000 A
6086657 Freije Jul 2000 A
6090189 Wikstrom et al. Jul 2000 A
6117216 Loreth Sep 2000 A
6118645 Partridge Sep 2000 A
6126722 Mitchell et al. Oct 2000 A
6126727 Lo Oct 2000 A
6149717 Satyapal et al. Nov 2000 A
6149815 Sauter Nov 2000 A
6152146 Taylor et al. Nov 2000 A
6163098 Taylor et al. Dec 2000 A
6176977 Taylor et al. Jan 2001 B1
6182461 Washburn et al. Feb 2001 B1
6182671 Taylor et al. Feb 2001 B1
6187271 Lee et al. Feb 2001 B1
6193852 Caracciolo et al. Feb 2001 B1
6203600 Loreth Mar 2001 B1
6212883 Kang Apr 2001 B1
6228149 Alenichev et al. May 2001 B1
6251171 Marra et al. Jun 2001 B1
6252012 Egitto et al. Jun 2001 B1
6270733 Rodden Aug 2001 B1
6277248 Ishioka et al. Aug 2001 B1
6282106 Grass Aug 2001 B2
D449097 Smith et al. Oct 2001 S
D449679 Smith et al. Oct 2001 S
6296692 Gutmann Oct 2001 B1
6302944 Hoenig Oct 2001 B1
6309514 Conrad et al. Oct 2001 B1
6312507 Taylor et al. Nov 2001 B1
6315821 Pillion et al. Nov 2001 B1
6328791 Pillion et al. Dec 2001 B1
6348103 Ahlborn et al. Feb 2002 B1
6350417 Lau et al. Feb 2002 B1
6362604 Cravey Mar 2002 B1
6372097 Chen Apr 2002 B1
6373723 Wallgren et al. Apr 2002 B1
6379427 Siess Apr 2002 B1
6391259 Malkin et al. May 2002 B1
6398852 Loreth Jun 2002 B1
6447587 Pillion et al. Sep 2002 B1
6451266 Lau et al. Sep 2002 B1
6464754 Ford Oct 2002 B1
6471753 Ahn et al. Oct 2002 B1
6494940 Hak Dec 2002 B1
6497754 Joannou Dec 2002 B2
6504308 Krichtafovitch et al. Jan 2003 B1
6506238 Endo Jan 2003 B1
6508982 Shoji Jan 2003 B1
6544485 Taylor Apr 2003 B1
6576046 Pruette et al. Jun 2003 B2
6585935 Taylor et al. Jul 2003 B1
6588434 Taylor et al. Jul 2003 B2
6603268 Lee Aug 2003 B2
6613277 Monagan Sep 2003 B1
6632407 Lau et al. Oct 2003 B1
6635105 Ahlborn et al. Oct 2003 B2
6635106 Katou et al. Oct 2003 B2
6672315 Taylor et al. Jan 2004 B2
6680028 Harris Jan 2004 B1
6709484 Lau et al. Mar 2004 B2
6713026 Taylor et al. Mar 2004 B2
6735830 Merciel May 2004 B1
6749667 Reeves et al. Jun 2004 B2
6753652 Kim Jun 2004 B2
6761796 Srivastava et al. Jul 2004 B2
6768108 Hirano et al. Jul 2004 B2
6768110 Alani Jul 2004 B2
6768120 Leung et al. Jul 2004 B2
6768121 Horsky Jul 2004 B2
6770878 Uhlemann et al. Aug 2004 B2
6774359 Hirabayashi et al. Aug 2004 B1
6777686 Olson et al. Aug 2004 B2
6777699 Miley et al. Aug 2004 B1
6777882 Goldberg et al. Aug 2004 B2
6781136 Kato Aug 2004 B1
6785912 Julio Sep 2004 B1
6791814 Adachi et al. Sep 2004 B2
6794661 Tsukihara et al. Sep 2004 B2
6797339 Akizuki et al. Sep 2004 B2
6797964 Yamashita Sep 2004 B2
6799068 Hartmann et al. Sep 2004 B1
6800862 Matsumoto et al. Oct 2004 B2
6803585 Glukhoy Oct 2004 B2
6805916 Cadieu Oct 2004 B2
6806035 Atireklapvarodom et al. Oct 2004 B1
6806163 Wu et al. Oct 2004 B2
6806468 Laiko et al. Oct 2004 B2
6808606 Thomsen et al. Oct 2004 B2
6809310 Chen Oct 2004 B2
6809312 Park et al. Oct 2004 B1
6809325 Dahl et al. Oct 2004 B2
6812647 Cornelius Nov 2004 B2
6815690 Veerasamy et al. Nov 2004 B2
6818461 Amami et al. Nov 2004 B2
6818909 Murrell et al. Nov 2004 B2
6819053 Johnson Nov 2004 B2
6855190 Nikkhah Feb 2005 B1
6863869 Lau et al. Mar 2005 B2
6893618 Kotlyar et al. May 2005 B2
6897617 Lee May 2005 B2
6899745 Gatchell et al. May 2005 B2
6908501 Reeves et al. Jun 2005 B2
6911186 Taylor et al. Jun 2005 B2
6958134 Taylor et al. Oct 2005 B2
6974560 Taylor et al. Dec 2005 B2
6984987 Taylor et al. Jan 2006 B2
7056370 Reeves et al. Jun 2006 B2
7097695 Lau et al. Aug 2006 B2
7220295 Lau et al. May 2007 B2
7244289 Su Jul 2007 B2
7404935 Lau et al. Jul 2008 B2
20010004046 Taylor et al. Jun 2001 A1
20010048906 Lau et al. Dec 2001 A1
20020069760 Pruette et al. Jun 2002 A1
20020079212 Taylor et al. Jun 2002 A1
20020098131 Taylor et al. Jul 2002 A1
20020100488 Taylor et al. Aug 2002 A1
20020122751 Sinaiko et al. Sep 2002 A1
20020122752 Taylor et al. Sep 2002 A1
20020127156 Taylor Sep 2002 A1
20020134664 Taylor et al. Sep 2002 A1
20020134665 Taylor et al. Sep 2002 A1
20020141914 Lau et al. Oct 2002 A1
20020144601 Palestro et al. Oct 2002 A1
20020146356 Sinaiko et al. Oct 2002 A1
20020150520 Taylor et al. Oct 2002 A1
20020152890 Leiser Oct 2002 A1
20020155041 McKinney, Jr. et al. Oct 2002 A1
20020170435 Joannou Nov 2002 A1
20020190658 Lee Dec 2002 A1
20020195951 Lee Dec 2002 A1
20030005824 Katou et al. Jan 2003 A1
20030170150 Lau et al. Sep 2003 A1
20030196887 Lau et al. Oct 2003 A1
20030206837 Taylor et al. Nov 2003 A1
20030206839 Taylor et al. Nov 2003 A1
20030206840 Taylor et al. Nov 2003 A1
20030233935 Reeves et al. Dec 2003 A1
20040033176 Lee et al. Feb 2004 A1
20040047775 Lau et al. Mar 2004 A1
20040052700 Kotlyar et al. Mar 2004 A1
20040065202 Gatchell Apr 2004 A1
20040096376 Taylor et al. May 2004 A1
20040136863 Yates et al. Jul 2004 A1
20040166037 Youdell et al. Aug 2004 A1
20040226447 Lau et al. Nov 2004 A1
20040234431 Taylor et al. Nov 2004 A1
20040251124 Lau Dec 2004 A1
20050000793 Taylor et al. Jan 2005 A1
20050223898 Nikkhah Oct 2005 A1
Foreign Referenced Citations (34)
Number Date Country
87210843 Jul 1988 CN
2111112 Jul 1992 CN
2138764 Jun 1993 CN
2153231 Dec 1993 CN
2174002 Aug 1994 CN
2206057 Aug 1973 DE
19741621 Jun 1999 DE
0433152 Jun 1991 EP
2690509 Oct 1993 FR
643363 Sep 1950 GB
S 63164948 Aug 1988 JP
S 5190077 Jul 1993 JP
S 6220653 Aug 1994 JP
10137007 May 1998 JP
11104223 Apr 1999 JP
2000236914 Sep 2000 JP
WO 8803057 May 1988 WO
WO 9205875 Apr 1992 WO
WO 9604703 Feb 1996 WO
WO 9907474 Feb 1999 WO
WO 0010713 Mar 2000 WO
WO 0147803 Jul 2001 WO
WO 0148781 Jul 2001 WO
WO 0164349 Sep 2001 WO
WO 0185348 Nov 2001 WO
WO 0220162 Mar 2002 WO
WO 0220163 Mar 2002 WO
WO 0230574 Apr 2002 WO
WO 0232578 Apr 2002 WO
WO 0242003 May 2002 WO
WO 02066167 Aug 2002 WO
WO 03009944 Feb 2003 WO
WO 03013620 Feb 2003 WO
WO 03013734 Feb 2003 WO
Non-Patent Literature Citations (4)
Entry
Lentek Sila™ Plug-In Air Purifier/Deodorizer product box copyrighted 1999.
“Zenion Elf Device,” drawings, prior art, 1 page.
Electrical Schematic and promotional material available from Zenion Industries, 7 pages, Aug. 1990.
Promotional material available from Zenion Industries for the Plasma-Tron, 2 pages, Aug. 1990.
Related Publications (1)
Number Date Country
20120097028 A1 Apr 2012 US
Provisional Applications (2)
Number Date Country
60341090 Dec 2001 US
60306479 Jul 2001 US
Continuations (4)
Number Date Country
Parent 12723102 Mar 2010 US
Child 13112873 US
Parent 10074209 Feb 2002 US
Child 12723102 US
Parent 09186471 Nov 1998 US
Child 09730499 US
Parent 09564960 May 2000 US
Child 09924624 US
Continuation in Parts (3)
Number Date Country
Parent 09730499 Dec 2000 US
Child 10074209 US
Parent 09924624 Aug 2001 US
Child 10074209 Feb 2002 US
Parent 09186471 Nov 1998 US
Child 09564960 US