1. Field of the Art
The present invention relates to devices and methods for creating cold plasmas, and, more particularly, to cold plasma sterilization methods and application devices.
2. Background Art
Atmospheric pressure hot plasmas are known to exist in nature. For example, lightning is an example of a DC arc (hot) plasma. Many DC arc plasma applications have been achieved in various manufacturing processes, for example, for use in forming surface coatings. Atmospheric pressure cold plasma processes are also known in the art. Most of the at or near atmospheric pressure cold plasma processes are known to utilize positive to negative electrodes in different configurations, which release free electrons in a noble gas medium.
Devices that use a positive to negative electrode configuration to form a cold plasma from noble gases (helium, argon, etc.) have frequently exhibited electrode degradation and overheating difficulties through continuous device operation. The process conditions for enabling a dense cold plasma electron population without electrode degradation and/or overheating are difficult and challenging to achieve.
In another challenging area, autoclaves continue to be used for sterilization of hospital equipment, particularly surgical instruments. However, the use of autoclaves poses several disadvantages that include the following. First, the time needed to cycle an autoclave system (e.g., up to 45 minutes for a full cycle) is substantial, and includes the need for significant cool down time. Second, the repeated temperature swings are rough on equipment, and the use of steam weathers metals. Third, autoclaves are large pieces of equipment with high upkeep costs and frequent downtime. Finally, when a surgical instrument is dropped or otherwise contaminated in an operating room, it must be “flashed” in the autoclave. This is a short cycle (e.g. 15-20 minutes) of high heat and pressure. These surgical instruments come back to the operating room very hot and therefore must cool prior to their use. During this time period, the patient is under anesthetic and likely has an opened wound, with resulting increased potential complications. It is therefore desirable to have an improved method of rapidly sterilizing surgical instruments without the undesirable heating effects, exposure to steam and length time periods associated with autoclaves.
As noted above, autoclaves have a number of disadvantages in their use in the sterilization of medical equipment. It is therefore desirable to have an improved method of rapidly sterilizing surgical instruments without the undesirable heating effects and exposure to steam.
Non-thermal gas plasmas (i.e., cold plasmas) have been shown to be effective at the destruction of many pathogens. In addition to their usefulness in the destruction of pathogens, it is also desirable to recirculate the gas used for cold plasma generation. Recirculation not only increases the efficiency of a cold plasma system, but also reduces the operating costs of such a system. In order to achieve effective sterilization of surfaces, and more specifically surgical instruments, contact times of several minutes may be necessary. To effect longer contact times, it is desirable to have a chamber that can contain one or more instruments and a volume of plasma. This description embodies the concept, in device and technique, for creating a plasma sterilization chamber and recirculating the feed/source specialty gas which would otherwise be lost to ambient air conditions. The contained CP recirculation unit shows how a noble gas can be used repeatedly in a cold plasma reaction chamber by way of electron separation in the reaction chamber, and electron attraction back to the normal atomic orbit in the non-energized part of the recirculation unit. This system works at or near atmospheric pressure levels, requiring no substantial additional pressure or vacuum.
An embodiment of a cold plasma sterilization device is described that includes a plasma chamber having a gas input port and a gas output port for throughput of a gas. One or more dielectric barrier discharge devices are attached to the plasma chamber and are configured to generate a cold plasma within the plasma chamber. Each of the one or more dielectric barrier discharge devices is formed by a dielectric barrier being sandwiched between a respective electrode and the interior of the plasma chamber. In addition, each of the electrodes is coupled to a high voltage electric input. A conductive stand is disposed within the plasma chamber and configured to accept an object for sterilization, wherein the conductive stand is coupled to ground. In a further embodiment, recirculation of the gas in the cold plasma sterilization device is described.
Another embodiment is described regarding a method of generating a cold plasma. An object for sterilization is placed on a conductive stand inside a plasma chamber, where the conductive stand is coupled to ground and configured to accept the object for sterilization. The plasma chamber includes a gas input port and a gas exit port. Gas is received into the plasma chamber via a gas input port, with the gas exiting via a gas output port. The gas is energized in the plasma chamber to generate a cold plasma via one or more dielectric barrier discharge devices attached to the plasma chamber. A dielectric barrier is sandwiched between an electrode and the interior of the plasma chamber to form each of the one or more dielectric barrier discharge devices. Each of the electrodes is coupled to a high voltage electric input.
Cold temperature atmospheric pressure plasmas have attracted a great deal of enthusiasm and interest by virtue of their provision of plasmas at relatively low gas temperatures. The provision of a plasma at such a temperature is of interest to a variety of applications, including wound healing, anti-bacterial processes, various other medical therapies and sterilization.
To achieve a cold plasma, a cold plasma device typically takes as input a source of appropriate gas and a source of high voltage electrical energy, and outputs a plasma plume.
The '369 application family describes a cold plasma device that is supplied with helium gas, connected to a high voltage energy source, and which results in the output of a cold plasma. The temperature of the cold plasma is approximately 65-120 degrees F. (preferably 65-99 degrees F.), and details of the electrode, induction grid and magnet structures are described. The voltage waveforms in the device are illustrated at a typical operating point in '369 application family.
In a further embodiment to that described in the '369 application, plasma is generated using an apparatus without magnets, as illustrated in
In both a magnet and a magnet-free embodiment, the inductance grid 66 is optional. When inductance grid 66 is present, it provides ionization energy to the gas as the gas passes by. Thus, although the inductance grid 66 is optional, its presence enriches the resulting plasma.
As noted above, the inductance grid 66 is optional. When absent, the plasma will nevertheless transit the cold plasma device and exit at the nozzle 68, although in this case, there will be no additional ionization energy supplied to the gas as it transits the latter stage of the cold plasma device.
As noted with respect to other embodiments, magnetic fields can be used in conjunction with the production of cold plasmas. Where present, magnetic fields act, at least at some level, to constrain the plasma and to guide it through the device. In general, electrically charged particles tend to move along magnetic field lines in spiral trajectories. As noted elsewhere, other embodiments can comprise magnets configured and arranged to produce various magnetic field configurations to suit various design considerations. For example, in one embodiment as described in the previously filed '369 application family, a pair of magnets may be configured to give rise to magnetic fields with opposing directions that act to confine the plasma near the inductance grid.
The '369 application family also illustrates an embodiment of the unipolar high voltage power supply architecture and components used therein. The circuit architecture is reproduced here as
Continuing to refer to
The quenching gap 360 is a component of the unipolar high voltage power supply 310. It modulates the push/pull of electrical energy between the capacitance banks, with the resulting generation of electrical energy that is rich in harmonic content. The quenching gap can be accomplished in a number of different ways, including a sealed spark gap and an unsealed spark gap. The sealed spark gap is not adjustable, while unsealed spark gaps can be adjustable. A sealed spark gap can be realized using, for example, a DECI-ARC 3000 V gas tube from Reynolds Industries, Inc. Adjustable spark gaps provide the opportunity to adjust the output of the unipolar high voltage power supply and the intensity of the cold plasma device to which it is connected. In a further embodiment of the present invention that incorporates a sealed (and therefore non-adjustable) spark gap, thereby ensuring a stable plasma intensity.
In an exemplary embodiment of the unipolar high voltage power supply, a 555 timer 320 is used to provide a pulse repetition frequency of approximately 150-600 Hz. As discussed above, the unipolar high voltage power supply produces a series of spark gap discharge pulses based on the pulse repetition frequency. The spark gap discharge pulses have a very narrow pulse width due to the extremely rapid discharge of capacitive stored energy across the spark gap. Initial assessments of the pulse width of the spark gap discharge pulses indicate that the pulse width is approximately 1 nsec. The spark gap discharge pulse train can be described or modeled as a filtered pulse train. In particular, a simple resistor-inductor-capacitor (RLC) filter can be used to model the capacitor, high voltage coil and series resistance of the unipolar high voltage power supply. In one embodiment of the invention, the spark gap discharge pulse train can be modeled as a simple modeled RLC frequency response centered in the range of around 100 MHz. Based on the pulse repetition frequency of 192 Hz, straightforward signal analysis indicates that there would be approximately 2,000,000 individual harmonic components between DC and 400 MHz.
In another embodiment of the unipolar high voltage power supply described above, a 556 timer or any timer circuit can be used in place of the 555 timer 320. In comparison with the 555 timer, the 556 timer provides a wider frequency tuning range that results in greater stability and improved cadence of the unipolar high voltage power supply when used in conjunction with the cold plasma device.
Devices, other than the cold plasma device illustrated above in
In an exemplary embodiment of the present invention, a sterilization device is provided as shown in
As noted above, plasma chamber 510 is a chamber in which gas of an appropriate composition can be presented for gas flow through to an output orifice, such as gas output 550. In a typical example, the gas is helium. Other gases include a helium-oxygen gas combination, although other gases and gas combinations can be used. When electrical energy is applied to device, a cold plasma is formed in the gas. Stray capacitance in plasma chamber 510 will flow to ground to complete the electrical circuit and result in the formation of ionized gas or plasma (albeit somewhat diffuse). A target object (e.g., an object to be sterilized) can be placed in an object holder within plasma chamber 510. If the object holder has a connection, or a suitable capacitance, to ground, such a connection will result in a greater intensity of the plasma. The cold plasma can be visual in that a non-transparent color will become evident upon the provision of energy to the gas. This type of cold plasma device can be used for the sterilization of surgical implants and instruments, where a small size model is suitable for use in operating room, laboratory, medical office, etc., and a large size model is suitable for central sterilization processing in a hospital, medical supply or manufacturing facility.
Gas can be used once and released. Alternatively, the gas can be re-used or recycled (i.e., recirculated). Advantages obtained by recirculating the gas include the following. First, gases, and in particular noble gases such as helium, are expensive. Second, power utilization can be reduced. Fresh gas that enters the system for the first time requires high energy levels to achieve ionization, while returning gas in a recirculation system retains an elevated energy level when it returns to the plasma chamber. Consequently, recirculation allows for potentially a lower power consumption. Third, certain working environments do not permit large volumes of gas (e.g., noble gas) in a contained occupied space such as an operating room due to the risk of potential suffocation. Furthermore, when an ionized noble gas mixes with ambient air, reactive molecules such as ozone are produced, which are potential irritants. Finally, a recirculation process causes turbulence that ensures the cold plasma is well distributed in the treatment chamber, and therefore reaches into the inner lumina of tools (e.g., cannulated drill bits, laparoscopy tools).
In an exemplary embodiment of the present invention, a low gas consumption embodiment 600 of the cold plasma device is illustrated in
A typical use model of the cold plasma sterilization system 600 is described below. An object, such as a medical instrument, to be sterilized is placed into plasma chamber 620. A suitable gas source, such as a noble gas source is connected to the fill port 650 and both the fill port 650 and exit port 660 are opened until plasma chamber 620 contains only noble gas. At this point, fill port 650 and exit port 660 are both closed. The electrical energy is next provided to electrical input 680, which is coupled to electrodes similar to electrodes 520 illustrated in
Referring to
Referring to both
In a further embodiment, plasma chambers 610 can be configured in series to allow multiple simultaneous objects to be sterilized in a row of chambers, all connected to the same recirculatory gas system. A bypass port and valve assembly could accompany each chamber so that if one chamber were to be opened, the power is cut, and gas is bypassed so that the other chambers remain unaffected. Once closed again, the individual chamber is purged with fresh noble gas, valves opened, and it is returned to the series. Such a multiple plasma chamber configuration would be useful for high throughput applications.
In a still further embodiment, plasma chamber 510 can include doors or flaps at the gas input 540 and gas output 550. Before accessing plasma chamber 510, the doors or flaps can be closed on the inflow and outflow tubes of plasma chamber 510 in order to seal off the rest of the system from the ambient environment. After the next item is loaded in plasma chamber 510, the chamber is purged with fresh gas, and the doors or flaps are then reopened. Using the doors or flaps, only plasma chamber 510 needs to be purged and refilled with the gas, rather than the whole system. Alternatively, fill port 650 and exit port 660 can be located anywhere in the system, including at the plasma chamber 510. Therefore, instead of doors or flaps, fill port 650 and exit port 660 can be used to purge plasma chamber 510. For example, a gas cartridge can be connected to fill port 650 to refill plasma chamber 510. Using this approach, the gas in the remainder of the system (i.e., the gas that is “walled off”) would take a substantial amount of time to become sufficiently contaminated as to adversely affect the cold plasma generation process, and thereby require more extensive purging. Using the doors or flaps thereby reduces gas consumption. In a hospital sterilization setting, small gas cartridges can be used rather than large gas cylinders to supply gas to the cold plasma sterilization system.
The process begins at step 1010. In step 1010, an object for sterilization is placed on a metal stand inside a plasma chamber, wherein the conductive stand is coupled to ground and configured to accept an object for sterilization, and wherein the plasma chamber includes a gas input port and a gas exit port. In an embodiment, an object 820 is placed on a conductive stand 740 in a plasma chamber 710, having gas input and output ports 750, 760.
In step 1020, gas is received into a plasma chamber. In an embodiment, a gas is received into plasma chamber 710.
In step 1030, the received gas is energized in the plasma chamber to form a cold plasma via one or more dielectric barrier discharge devices attached to the plasma chamber, wherein each of the one or more dielectric barrier discharge devices is formed by a dielectric barrier being sandwiched between an electrode and the interior of the plasma chamber, and wherein each of the electrodes is coupled to a high voltage electric input. In an embodiment, the received gas is energized in plasma chamber 710 using energy from electrodes 720 that is in turn received from electrical input 730. Dielectric barrier 560 is sandwiched between electrode 520 and plasma chamber 510.
At step 1040, method 1000 ends.
The process begins at step 1110. In step 1110, an object for sterilization is placed on a metal stand inside a plasma chamber, wherein the conductive stand is coupled to ground and configured to accept an object for sterilization, and wherein the plasma chamber includes a gas input port and a gas exit port. In an embodiment, an object 820 is placed on a conductive stand 740 in a plasma chamber 710, having gas input and output ports 750, 760.
In step 1120, gas is received into a plasma chamber. In an embodiment, a gas is received into plasma chamber 710.
In step 1130, the received gas is energized in the plasma chamber to form a cold plasma via one or more dielectric barrier discharge devices attached to the plasma chamber, wherein each of the one or more dielectric barrier discharge devices is formed by a dielectric barrier being sandwiched between an electrode and the interior of the plasma chamber, and wherein each of the electrodes is coupled to a high voltage electric input. In an embodiment, the received gas is energized in plasma chamber 710 using energy from electrodes 720 that is in turn received from electrical input 730. Dielectric barrier 560 is sandwiched between electrode 520 and plasma chamber 510.
In step 1140, flaps in the plasma chamber are closed to seal the plasma chamber.
In an embodiment, flaps in plasma chamber 710 are closed to thereby suspend gas recirculation.
In step 1150, the plasma chamber is purged with fresh gas. In an embodiment, plasma chamber 710 is purged with fresh gas with, for example, the use of a gas cartridge to provide the required amount of gas.
In step 1160, the flaps in the plasma chamber are reopened. In an embodiment, flaps in plasma chamber 710 are reopened to thereby resume gas recirculation.
In step 1170, method 1100 ends.
It is to be appreciated that the Detailed Description section, and not the Summary and Abstract sections, is intended to be used to interpret the claims. The Summary and Abstract sections may set forth one or more but not all exemplary embodiments of the present invention as contemplated by the inventor(s), and thus, are not intended to limit the present invention and the appended claims in any way.
The present invention has been described above with the aid of functional building blocks illustrating the implementation of specified functions and relationships thereof. The boundaries of these functional building blocks have been arbitrarily defined herein for the convenience of the description. Alternate boundaries can be defined so long as the specified functions and relationships thereof are appropriately performed.
The foregoing description of the specific embodiments will so fully reveal the general nature of the invention that others can, by applying knowledge within the skill of the art, readily modify and/or adapt for various applications such specific embodiments, without undue experimentation, without departing from the general concept of the present invention. Therefore, such adaptations and modifications are intended to be within the meaning and range of equivalents of the disclosed embodiments, based on the teaching and guidance presented herein. It is to be understood that the phraseology or terminology herein is for the purpose of description and not of limitation, such that the terminology or phraseology of the present specification is to be interpreted by the skilled artisan in light of the teachings and guidance.
The breadth and scope of the present invention should not be limited by any of the above-described exemplary embodiments, but should be defined only in accordance with the following claims and their equivalents.
The present application claims the benefit under 35 U.S.C. §119(e) of U.S. Provisional Patent Application No. 61/535,250, entitled “Harmonic Cold Plasma Devices and Associated Methods”, filed on Sep. 15, 2011, which is hereby expressly incorporated by reference in its entirety. This application is related to U.S. patent application Ser. No. 13/149,744, filed May 31, 2011, U.S. patent application Ser. No. 12/638,161, filed Dec. 15, 2009, U.S. patent application Ser. No. 12/038,159, filed Feb. 27, 2008, and U.S. Provisional Application No. 60/913,369, filed Apr. 23, 2007, each of which are herein incorporated by reference in their entireties.
Number | Date | Country | |
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61535250 | Sep 2011 | US |