It is well known that pathogens, allergens and other airborne contaminants including pathogenic microbes, pollutants, viruses and other microorganisms cause a number of health hazards. In particular, in indoor spaces each time an occupant of that indoor space exhales or sneezes, microorganisms are carried into the indoor air that is ultimately breathed in by others. With the recent outbreak of COVID-19, which is caused by the SARS-CoV-2 virus, the importance of reducing, and if possible removing pathogens from indoor environments in which humans live, work and otherwise occupy has received much recent attention. Known efforts to reduce pathogens and/or microbes in an indoor environment typically are associated with the use of components connected to and used within existing HVAC systems that supply air to an indoor space.
Embodiments herein include systems and methods for reducing the pathogen load in an indoor space. Embodiments also include systems and methods for preventing air expelled by humans from entering an indoor space. The systems and methods described herein include systems for eliminating, or at least reducing pathogens including harmful microbes, viruses and other life-threatening pathogens in an indoor space. Pathogens, as used herein, is intended to include harmful microbes and viruses including but not limited to SARS CoV-2. The systems and methods described herein operate independent of existing HVAC systems used to condition the air in an indoor space, and do not connect to or use the ductwork or other components of HVAC systems.
Referring now to the figures,
System 5 further includes a plurality of updraft hoods 25 which may be referred to as updraft cubicles. Air conduits 32 connect updraft hoods 25 with the air duct 10 through inlets 20 defined therein. In the embodiment described updraft hoods 25 may comprise updraft cubicles with an outer wall 34 and an open bottom 36. A side opening 38 is defined in the outer wall which will allow the entry and exit of a human operator positioned at a work station or other location occupiable by humans. The updraft cubicle in the described embodiment is generally rectangularly shaped in cross section, but is not limited to such a shape. If desired, updraft hoods 25 may have a curtain or wall that covers the opening 38 such that the only opening for the updraft hoods 25 once occupied is the open bottom 36.
A burn zone 40 is communicated with air duct 10. Burn zone 40 may comprise a burner 42 with outer housing 48 that defines an interior 43 therein. Burner 42 is heatable to a high temperature. In one embodiment burner 42 may comprise a media 44 in an outer housing 48. The media will be of a type that can be heated to and maintain high temperatures of as much as 500° F. In some embodiments the media can be heated to as much as 600° F., 700° F., 800° F., 900° F. and up to 1000° F. The media may comprise for example a ceramic material or metal beads. The media will in all cases be porous, or will otherwise define a travel path through the burner 42 to allow the flow of air therethrough.
A heating element 46 such as for example an electric coil may also be disposed in the outer housing 48 of burner 42. Other known means of heating may be utilized, such as an induction coil placed proximate a metal rod or other metal object placed in the interior 43. Outer housing 48 can be comprised of a material that will withstand high temperatures without emitting excessive heat to the surrounding area. The outer housing may also have an insulating material therearound to insulate burner 42. The heated air stream leaving burner 42 will have reduced pathogens as compared to the contaminated air entering the burner 42, and will be cooled as described below.
A connecting duct 50 communicates burn zone 40 with a scrubber 52. Scrubber 52 serves a dual purpose in that air passing therethrough will go through a spray of vapor in one embodiment, or in another embodiment will pass through a fill media over which water circulates. In this manner the air can be cooled and filtered at the same time. The water may in some cases be chemically treated such that it may comprise for example chlorinated water at pH levels that are equal or similar to those recommended for public swimming pools. Scrubber 52 is therefore also referred to as a cooling apparatus. A pump (not shown) may circulate water across a fill media in scrubber 52 to allow the air to be cooled and scrubbed. It is not necessary to provide any chemical treatment to the water such that the water may simply be used as a cooling agent. A fresh air damper 51 may be included in connecting duct 50. Fresh air from the indoor space may be drawn into the connecting duct 50 through fresh air damper 51 to aid in cooling the heated air stream exiting burner 42.
Additional cooling may be supplied by a heat exchanger 56 as schematically shown in
A cooled air stream leaves scrubber 52 and enters the UV chamber at a tangent 62 so that a centrifugal motion is created. Air will move in a centrifugal manner around the inner wall of the UV chamber 60. Ultraviolet lights 64 may be inserted and extend into an interior 61 of UV chamber 60. UV chamber 60 may also include a plurality of UV lights arranged in a spiral fashion along the interior 61. In the schematic of
A connecting conduit 72 communicates UV chamber 60 with a blower, or pump 70 of a type known in the art. Blower 70 will operate to create a negative pressure, or soft vacuum at air inlets 20. As a result, air will be pulled into air duct 10 through updraft hoods 25. Updraft hoods 25 are positioned at human occupiable locations. Human occupiable locations as used herein means those places in a room or building that in a typical situation are occupied by humans, such as a work station, a desk, seating at a restaurant or in an office area. By strategically locating updraft hoods 25 at such locations, the system 5 can prevent pathogen laden air expelled by a human in those locations from ever entering the indoor space outside the updraft hood. At least a portion of the air expelled by the human will be contained within the updraft hood and passed into the system 5 for treatment as described, and in some cases all of the air expelled by the human will be contained within the updraft hood and passed into the system 5.
A human worker in the updraft hood 25 will expel air through normal exhalation, coughing, sneezing, talking and other bodily functions that require air to be expelled through the nose or the mouth. The vacuum created by the pump 70 should be at a level sufficient to pull the majority of the air, and in some cases all of the air expelled by the human positioned in the updraft hood 25. Any pathogens in the expelled air pulled into the air duct 10 will be treated and conditioned as described. In this way, pathogens expelled by humans are prevented from ever entering indoor space 6 and contaminating the air therein. Air is pulled into air duct 10 and communicated through the burn zone 40. In one embodiment temperature in the burn zone exceeds 500° F. degrees. In additional embodiments the temperature in the burn zone is between 500 and 1,000° F. In other embodiments, the temperature may be between 500° F. and 900° F., 500° F. and 800° F., 500° F. and 700° F., and 500° F. and 600° F. and any ranges therebetween. In any event, burner 42 is configured to heat the burn zone to an internal temperature of as much as 1,000° F. The heated air stream leaving the burner 42 may likewise reach the foregoing temperatures. The treated air leaving burner 42 will have a reduced pathogen load as compared to the contaminated air. The cooled, treated air stream is delivered into the indoor space through an air exit 74 at, or near the ambient temperature of the indoor space.
As is understood from the drawings a method of removing pathogens may comprise positioning a plurality of air inlets at a plurality of locations in the indoor space. The method may further include pulling indoor air into the air inlets 20 and passing the indoor air through a burner 42 having an internal temperature sufficient to eliminate, or at least significantly reduce pathogens in the air passing through the burner. The method may comprise exposing the air to high temperatures for a short period of time at the high temperature. In one embodiment the method may comprise exposing the air in a burner to temperature ranges noted above for no more than three seconds to eliminate, or at least reduce the pathogens that existed in the air prior to the exposure to the temperatures in the burner. In a specific embodiment, the method includes exposing the air to a temperature range of between about 517° F. and 662° F. for no more than 2.61 seconds.
The method may comprise passing the indoor air through a burner having an internal temperature of at least 500° F. to create a heated air stream. The method may comprise heating the indoor air to higher temperatures, for example 600° F., 700° F., 800° F., 900° F. or 1000° F. to create a heated air stream. The heated air stream may then be cooled to create a cooled air stream having a temperature about the same as the air in the indoor space. In one embodiment the temperature of the air will be not more than 10° F. different than the temperature of the air in the indoor space. The cooled air stream is then exhausted back into the indoor space. The method may further comprise exposing a cooled air stream to UV radiation prior to the exhausting step.
The cooling step may comprise for example injecting a vapor stream into the heated air stream after it leaves the burner, and/or passing the air through a heat exchanger and/or through a scrubber with fill media over which cool water flows. The method may also include preventing pathogens expelled from a human from entering indoor air space 6. The method includes placing an updraft hood 25 around at least the head of a human in the indoor space, and pulling the air emitted by the human from the updraft hood 25 through an air inlet into an air duct that communicates the air into the burner 42, The air is then treated and conditioned as described and is exhausted as treated air into the indoor air space. The treated air will be clean air, and will be free of pathogens or will at least have a reduced level of pathogens than existed in the contaminated air.
In the embodiment described in
Air may be communicated from indoor air space 101 through an air supply duct 104. Air will pass through a burner 106 which will reach temperatures sufficient such that pathogens in the air passing therethrough, such as in a non-limiting example SARS-CoV-2, will be eliminated or at least significantly reduced. A connecting conduit 108 connects burner 106 with a cooling apparatus 110. Cooling apparatus 110 may be for example a cooling tower with media over which water is sprayed. One embodiment may have a closed circuit cooling tower which may include a coil through which the heated air stream from burner 106 flows. Water will pass over the coils in the cooling tower to cool the heated air stream so that a cooled air stream exits cooling apparatus 110. Other cooling apparatus may be utilized to cool the heated air to create a cooled, treated air steam that will exit cooling apparatus 110 through a return air conduit 112. A UV chamber 114 includes a plurality of UV lamps, which may be UVC lamps, positioned therein. UV chamber 114 is connected in return air conduit 112. Return air conduit 112 may be divided into a first portion 113 and a second portion 116 so that the UV chamber separates the return air conduit into two portions. The cooled, treated air stream will pass through first portion 113 in return air conduit 112 and into the second portion 116 through UV chamber 114 where the air passing therethrough is directly exposed to UV radiation. The cooled air stream thus passes from return air conduit 112 into the indoor space 101. The cooled air stream entering the indoor space will be at about the same temperature of the air in the indoor space. In one embodiment the cooled air stream is at a temperature of no greater than 10° F. above the ambient air temperature in the indoor air space and in another no greater than 5° F.
An air pump 118 may be used to create a vacuum to pull the contaminated air from updraft hoods in the indoor space 101 through the system 102. All, or part of the system components including burner 106, cooling apparatus 110, UV chamber 114 and air pump 118 may be housed in a system building 119, or may be separately housed or simply positioned exterior to building 100.
As schematically depicted in
The operation of system 102 is generally the same as that with respect to system 5 only on a larger scale. Air pump 118 will create negative pressure at each of the air inlets 126 through conduits 32 and will pull air upwardly from updraft hoods 25 into duct branches 124 and air duct 122. Thus, air expelled by sneezes, exhalations or otherwise by any human operators in the updraft hoods 25 will be pulled upwardly along with any air that is pulled through the opening 38 from indoor space 101. As a result, the system 102 is not only a system that eliminates, or reduces pathogens, but is a system and method that prevents pathogens expelled by humans from entering and contaminating the air in indoor space 101. Air expelled by humans in updraft hoods 25, along with air from indoor space 101 that passes into updraft hoods 25 through the open side thereof, will pass through air duct 122 into the supply air duct 104 and into system 102. Burner 106 is configured such that the internal temperature will reach at least 500° F. In other embodiments the burner 106 is configured to reach internal temperatures of at least 600° F., 700° F., 800° F., 900° F., and as much as 1,000° F. Air passing though burner 106 will be exposed to the temperature in the burner 106, and exposing air to the temperatures described for burner 106 will reduce, and in most cases eliminate pathogens from the air passing therethrough. Based on the below described testing conducted on the impact of increased temperatures on MS-2, which is a surrogate for SARS-CoV-2, it is believed that exposing contaminated air to -elevated temperatures for a short period of time, for example as little as five seconds, and further as little as three seconds, will kill pathogens, and more specifically will kill SARS-CoV-2. It is likewise believed that the higher the temperature, the less residence time will be needed. Thus, it is believed that exposing the contaminated air to temperatures of above 500° F., for example as much 600° F., 700° F., 800° F., 900° F., and/or 1,000° F., and temperature ranges therebetween, may kill pathogens in contaminated air, and will do so with little residence, or exposure time. In one embodiment, air passing through a burner is exposed to an entry temperature of about 517° F. at the point of entry for the air into the burner and an exit temperature is about 662° F. The residence time for air passing through the burner may be less than three seconds, and in one example about 2.61 seconds.
A heated air stream will leave burner 106 and will begin to cool in the connecting duct 108 from the burner 106 to the cooling apparatus 110. The heated air stream will be cooled further by the cooling apparatus 110. The heated air stream will be cooled by cooling apparatus 110 to a temperature of not greater than 10° F. and preferably not greater than 5° F. over the ambient air temperature in the indoor space.
In one embodiment the updraft hoods 25 that are not occupied can be deactivated. One manner of doing this would be simply to have a valve in the conduits 32 that can be automatically controlled from a controller. In this way less power will be required to generate the air flow necessary to pull the air from activated updraft hoods. In addition, an updraft hood 25 can be movable from a lowered position in which it at least partially covers a human, to a raised position in which the updraft hood 25 is positioned above a human in the occupiable space 120.
Burner 106 can be for example a plurality of burners 42 as described earlier connected in series. Burner 106 may have other configurations capable of reaching the internal temperatures described herein. An example of a burner embodiment may be as described with respect to
Interior 140 may be separated into a dirty air plenum 150 in an upper portion thereof and a clean air plenum 152 in a lower portion thereof. In one embodiment dirty air plenum 150 may comprise a heated plenum. Dirty air plenum 150 may be heated by a gas fired fire box or other known methods.
Burner portion 168 has an outer housing 170 which may be a porous outer housing 170. In one embodiment the outer housing 170 may comprise a ceramic material. In the partial section view shown in
Outer housing 170 is filled with fill material 178 through which metal rods 172 extend. The fill material 178 may comprise metal beads, such as stainless steel beads or may comprise a ceramic or other material that can withstand temperatures of the ranges discussed herein and allow air to pass therethrough. The internal temperature of each of burner cylinder 158 will reach a minimum of at least 500° F., and in some embodiments 600° F., 700° F., 800° F., 900° F. and as much as 1,000° F. The operation of a system including the burner apparatus 106 is as described before. Pump 133 will pull air through burner inlet conduit 136 from air supply duct 104. Air will pass into interior 140 of silo 138 into the dirty air plenum 150. Air may be heated by a firebox or other heating mechanism in dirty air plenum 150. Air will be pulled through each of individual burner cylinders 158 and will be heated as it passes therethrough. The heated air stream will pass through outer housing 170 and into clean air plenum 152. A heated air stream will be communicated into a connecting conduit 177 and into a cooling apparatus 110 and UV chamber 114. Air will then be delivered into building 100 as previously described. The air will be heated to a temperature sufficient to eliminate, or at least significantly reduce pathogens from the contaminated air treated by the system 102. As explained below, tests have shown exposing air laden with MS-2 to high temperatures will eliminate, or at least dramatically reduce the MS-2 in the treated air. MS-2 is a bacteriophage that is accepted as a surrogate for SARS-CoV-2 and other pathogens and is more difficult to eliminate than SARS-CoV-2.
The temperature of each of burners 132 and 134 may be monitored and if the temperature to which the air is exposed in the burner 132, or if the temperature of the air leaving the burner falls below a specified temperature the valve 137 may be actuated so that the air from conduit 104 is redirected. For example, the air can be redirected from burner 132 to burner 134. The burner 132 will be heated to reach temperatures above the specified temperature as the contaminated air is directed to and heated by burner 134. The temperature at which the valve 137 will be actuated can be specified by the operator. For example, if the minimum desired temperature of the air leaving burner 132 is 500° F. and the temperature falls below 500° F., the valve 137 can be actuated to switch to burner 134. Rather than air temperature, the monitored temperature can be the internal temperature of the burner 132. This process can be continuous such that the temperatures to which the air is exposed and the air temperature leaving an individual burner can be monitored and the valve 137 actuated to switch back and forth between burners when the monitored temperature reaches a minimum specified temperature. Two burners are disclosed herein but it is understood that more than two may be utilized.
System 102, like the other systems disclosed herein, operate independent of existing HVAC systems, and are not connected thereto in any way. Although in the embodiment described in
Facility 190 has a plurality of human occupiable locations 192. Facility 190 is shown without a wall and a roof so that the indoor space 194 is visible. Locations 192 may be work stations, eating locations, or other locations occupiable by a human. At least one air duct 196, and in the embodiment described a plurality of air ducts 196 are positioned in indoor air space 194 and have air duct branches 198 extending outwardly and downwardly therefrom. The air ducts 196 may be communicated with and comprise part of an air treatment system as described herein, like for example air treatment system 102. Contaminated air from indoor space 194 drawn into and treated by the air treatment system 102 will be communicated back into the indoor air space 194.
In
Updraft hoods 304 are placed proximate a human occupiable space for example a chair in which a person may be seated. Air from indoor space 302 will be drawn into indoor air duct 306 and will be treated with a system as described herein. Air will be returned through a return air duct 308 connected to and communicated with the air treatment system. The air exhausted from return air duct 308 will contain fewer pathogens than the air drawn into hood 304. Air expelled by a person proximate the hood 304, or at least a portion thereof, will be pulled into hood 304, so that pathogens contained therein are prevented from entering the indoor space 302.
Test microorganisms were cultured, purified and concentrated prior to commencement. An MS-2 bacteriophage suspension was diluted to a starting concentration of 106 plaque forming units (PFU) per milliliter. Aerosols including the MS-2 were generated for five minutes while the test device was running and air was pumped through the test system. An atomizer was connected directly to the input 250 aerosolizing approximately 1.67 mL of the viral suspension. The output of the test device was piped into an ASTM chamber located in a chemical fume hood. Samples were collected using single stage Anderson viable impactor placed into the ASTM chamber. The device was operated for five minute runs. Samples were collected with each run along with temperature readings. The number of viable microorganisms were determined quantitatively using plaque counting techniques and converted to PFU/M2.
The burner section 252 of the test arrangement was a heating chamber of approximately four inches in diameter by twelve inches in length. The fill media in the heating chamber included 0.177 in. diameter metal beads heated by an electric heating coil. The inlet hose 250 was approximately ½ inch in diameter and air was pulled through the burner and through the system at approximately two cubic feet per minute. With a blower speed set at 2 cubic feet per minute or, 3456 cubic inches per minute within a volume of 0.087 cubic ft or, 150.72 cubic in and utilizing a magnehelic gauged vacuum reading of 0.75 inches the measured residence time of introduced continuous air plume was 2.61 seconds. In other words, the travel time for the air from the top of the burner to the bottom of the burner was 2.61 seconds. The UV chamber 260 included two T5 UVC tube light fixtures with ozone.
The results of eight trials are shown in
In addition, there are studies indicating that elevated temperatures may be effective to kill. SARS-CoV-2. SARS-CoV-2 is one of a number of coronaviruses, one of which is SARS-CoV which is closely related to SARS-CoV-2. Different studies have indicated that most coronaviruses would be killed after exposure to 149° F. for longer than three minutes. For temperatures lower than 149° F. indications were that longer exposure times were needed. At least one study estimated that SARS-CoV-2 would be killed after an average of 2.5 minutes at 158° F. Although the studies appear to have considered the impact of elevated temperature on surfaces, the correlation between the temperature and exposure time indicates that the higher the temperature, the less exposure time is required to eliminate SARS-CoV-2. Thus, it is believed that exposing contaminated air to significantly elevated temperatures, for example temperatures of 500° F. and higher as noted herein, should decrease the exposure time needed to eliminate, or at least significantly reduce pathogens in the contaminated air.
Thus, it is seen that the apparatus and methods of the present invention readily achieve the ends and advantages mentioned as well as those inherent therein. While certain preferred embodiments of the invention have been illustrated and described for purposes of the present disclosure, numerous changes in the arrangement and construction of parts and steps may be made by those skilled in the art, which changes are encompassed within the scope and spirit of the present invention.
This application claims the benefit of PCT Patent Application No. PCT/US2021/040304 filed Jul. 2, 2021, and U.S. Provisional Application No. 63/047,488 filed Jul. 2, 2020, which are hereby incorporated by reference.
Filing Document | Filing Date | Country | Kind |
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PCT/US2021/040304 | 7/2/2021 | WO |
Number | Date | Country | |
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63047488 | Jul 2020 | US |