Not applicable.
Not applicable.
1. Field of the Invention
This invention relates to the field of antimicrobials and more specifically to the field of hydrogen peroxide gas as an antimicrobial.
2. Background of the Invention
There is an increasing need for disinfection processes against bacteria, viruses, mold, and the like. Conventional disinfection processes involve the application of detergents and liquid sanitizers. Drawbacks to such conventional methods include inefficiencies disinfecting in certain locations such as between walls. Further drawbacks include inefficiencies in the frequency of the disinfection. For instance, such conventional disinfection processes are typically carried out on a daily basis or intermittently during a day.
Developments over such conventional processes include using hydrogen peroxide as a disinfectant. Disinfectant processes using hydrogen peroxide include vaporizing liquid hydrogen peroxide solutions to create a mist of water droplets containing hydrogen peroxide. Drawbacks include that such hydrogen peroxide mist may not be used in occupied spaces because the mist typically contains hundreds to thousands of parts per million of hydrogen peroxide. Further drawbacks include inefficiencies in disinfecting a volume of space because the droplets in the mist precipitate out of the air. Additional drawbacks include that the hydrogen peroxide in the mist is surrounded by water, which may insulate the hydrogen peroxide molecules in the droplets and may prevent the molecules from being drawn to the microbes in the air or on surfaces by electrostatic attraction.
Consequently, there is a need for an improved antimicrobial system for disinfection of surfaces and the air. Additional needs include an improved antimicrobial system using hydrogen peroxide.
These and other needs in the art are addressed in one embodiment by a purification device for producing hydrogen peroxide gas from air. The air comprises water vapor and oxygen. The purification device includes a body comprising an interior, an air inlet, and a gas outlet. The purification device also includes a catalyst. The catalyst is disposed within the interior. The catalyst comprises titanium dioxide. The purification device also includes a light disposed to emit electromagnetic radiation into the catalyst. In addition, the purification device includes a fan. The fan is disposed to blow air in a direction. The catalyst is disposed at an angle in relation to the direction.
In other embodiments, these and other needs in the art are addressed by a method of degrading microbes. The method includes feeding air to a catalyst. The catalyst comprises titanium dioxide. The air comprises water vapor and oxygen. The method also includes emitting electromagnetic radiation from a light, wherein the electromagnetic radiation contacts the catalyst. The method further includes reacting the air in the presence of the catalyst and the electromagnetic radiation to produce hydrogen peroxide gas. In addition, the method includes degrading the microbes with the hydrogen peroxide gas.
The foregoing has outlined rather broadly the features and technical advantages of the present invention in order that the detailed description of the invention that follows may be better understood. Additional features and advantages of the invention will be described hereinafter that form the subject of the claims of the invention. It should be appreciated by those skilled in the art that the conception and the specific embodiments disclosed may be readily utilized as a basis for modifying or designing other embodiments for carrying out the same purposes of the present invention. It should also be realized by those skilled in the art that such equivalent embodiments do not depart from the spirit and scope of the invention as set forth in the appended claims.
For a detailed description of the preferred embodiments of the invention, reference will now be made to the accompanying drawings in which:
As shown in
Catalyst 25 includes a light (not illustrated) disposed inside the catalyst body 110. The light is a non-ozone producing ultraviolet light. In embodiments, the light is a crystal ultraviolet light. Without limitation, commercial examples of non-ozone producing ultraviolet lights include the non ozone bulb provided by LightTech. Catalyst 25 includes one light. In alternative embodiments, catalyst 25 includes more than one light. The light is disposed to emit electromagnetic radiation into catalyst 25. For instance, the light emits electromagnetic radiation into the hexagonal, walled cells of catalyst 25 with the electromagnetic radiation contacting the surface of the cells. In alternative embodiments (not illustrated), the light is not disposed within catalyst 25 but is instead located out of catalyst 25 and disposed to emit electromagnetic radiation that contacts catalyst 25.
As shown in
In an embodiment as illustrated in
As further shown in the embodiments illustrated in
Without being limited by theory, the produced hydrogen peroxide gas has both positive and negative charges. With such charges, the hydrogen peroxide gas is drawn to microbes by electrostatic attraction. For instance, the hydrogen peroxide gas is drawn to the positive and negative charges of the surface of the microbes. The hydrogen peroxide gas then chemically degrades the microbes, which may be degraded cell by cell. In embodiments in which the microbes are attached to structures such as a wall, the hydrogen peroxide gas degrades the microbes down to the point of attachment. In some instances, the microbes release from the surface and may be removed. In embodiments, the microbes may be removed without removing structurally sound material. The hydrogen peroxide gas also diffuses into porous material (i.e., anywhere that air flows) such as porous walls and cloth, which allows degradation of the microbes behind the walls or in the cloth.
It is to be understood that purification device 5 is not limited to ambient air but in alternatives may use other suitable gases or vapors that contain water vapor and oxygen and that are suitable for producing hydrogen peroxide. For instance, a mixture of water vapor and oxygen may be provided to purification device 5 (i.e., by a tank).
The microbes may include any type of microbe. In an embodiment, the microbes comprise fungi, mold, viruses, bacteria, or any combinations thereof.
To further illustrate various illustrative embodiments of the present invention, the following examples are provided.
The effect of hydrogen peroxide produced from a purification device on the inactivation of Influenza A H1N1 (ATCC # VR-333) was evaluated. The virus culture was maintained on an ATCC complete growth medium and minimum essential medium (ATCC, Manassas, Va., USA) with 2 μM L-glutamine and Earle's BSS adjusted to contain 1.5 g/L sodium bicarbonate, 0.1 μM non-essential amino acids, and 1.0 μM sodium pyruvate. 90% fetal bovine serum, 10% cultured in Trypticase Soy Agar was added. Sodium bicarbonate, non-essential amino acids, and a combination of sodium pyruvate and fetal bovine serum, in aerobic growth conditions at 37.0° C. and Influenza A at 33-35° C. Cells from both of the above (approx. 1×107 CFU/ml) from a 24 hour static culture were incubated at 37.0° C., and Influenza A at 33-35° C. were used to inoculate various 5 cm×3 cm stainless steel coupons. The inoculum suspensions were enumerated by surface plating in duplicate samples on TSA after serial dilution in 0.1% peptone solution. The plates were incubated for 24 hour at 37.0° C.
A 100 μl droplet from the initial inoculum suspension of each of the bacteria/viruses was used to inoculate the external surface (6.3 cm×1.8 cm) on #8 stainless steel coupons. This resulted in a final inoculum level of approximately 7.0-log CFU/5 g sample. The inoculated samples were air dried for 1 hour at 22.0° C. prior to treatment with the no-ozone producing cell. The 1 hour drying allowed the inoculated cells to attach to the surface host and minimize the growth of inoculated cells during drying. Four stainless steel coupons were used for each sampling time.
A biocontainment chamber (BL 2 Enhanced) was equipped with a purification device and allowed to equilibrate for a period of two hours prior to placement of 12 inoculated coupons inside the chamber. The purification device used was a 14 inch cell. The cell was placed on the outside of the box, and the gases were blown into the container. The effect of the no-ozone producing cell treatment was measured at 0, 2, 4, 6, 8, 12 and 24 hours. A control study was conducted in the same chamber without the presence of the purification device. Temperature, relative humidity, and ambient ozone levels and hydrogen peroxide levels were monitored in the chamber.
After treatment, each of the 5 cm×3 cm coupons were transferred into a 400 ml stomacher bag (Fisher Scientific Inc., PA., USA) combined with 50 ml sterile 0.1% peptone solution, and then blended with a AES Easy Mix Stomacher (AES Laboratories, Princeton, N.J., USA) for 2 minutes at normal speed. Wash fluid was serially diluted, followed by surface plating for enumeration. A centrifugation method was used to recover low populations of injured viruses. The centrifugation method (Mossel and others 1991) was modified and used to concentrate the virus populations in the wash fluid so that less than 250 CFU/ml of the virus could be enumerated by the surface plating.
Table 1 summarizes the results of the example, which demonstrated the effectiveness of the purification device for the inactivation of Influenza A—H1N1. After 6 hours of treatment, levels of the H1N1 virus on inoculated stainless steel coupons were below the detection limit. No recovery was observed at 8, 12, or 24 hours.
The ambient ozone levels in the chamber containing the purification device were measured at 0.0055 ppm. Ozone levels in the control chamber were measured at 0.0050 ppm (no significant difference). Levels of vaporized hydrogen peroxide in the chamber equipped with the purification device ranged from 0.05-0.08 ppm. No vaporized H2O2 was measured in the control chamber. The relative humidity ranged from 47-59%, and the temperature from 70-72° F. in both the control and treated chambers.
The results indicated that the purification device was effective at inactivating Influenza A H1N1 virus on inoculated stainless coupons under the conditions of these tests.
Although the present invention and its advantages have been described in detail, it should be understood that various changes, substitutions and alterations may be made herein without departing from the spirit and scope of the invention as defined by the appended claims.