CN109589441B - Apparatus, system, and method for advanced oxidation process using photohydrogen ionization - Google Patents
Apparatus, system, and method for advanced oxidation process using photohydrogen ionization Download PDFInfo
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- CN109589441B CN109589441B CN201910048034.0A CN201910048034A CN109589441B CN 109589441 B CN109589441 B CN 109589441B CN 201910048034 A CN201910048034 A CN 201910048034A CN 109589441 B CN109589441 B CN 109589441B
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- advanced oxidation
- titanium dioxide
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Images
Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L9/00—Disinfection, sterilisation or deodorisation of air
- A61L9/16—Disinfection, sterilisation or deodorisation of air using physical phenomena
- A61L9/18—Radiation
- A61L9/20—Ultraviolet radiation
- A61L9/205—Ultraviolet radiation using a photocatalyst or photosensitiser
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L9/00—Disinfection, sterilisation or deodorisation of air
- A61L9/16—Disinfection, sterilisation or deodorisation of air using physical phenomena
- A61L9/22—Ionisation
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2101/00—Chemical composition of materials used in disinfecting, sterilising or deodorising
- A61L2101/02—Inorganic materials
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2101/00—Chemical composition of materials used in disinfecting, sterilising or deodorising
- A61L2101/02—Inorganic materials
- A61L2101/26—Inorganic materials containing copper
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2209/00—Aspects relating to disinfection, sterilisation or deodorisation of air
- A61L2209/20—Method-related aspects
- A61L2209/21—Use of chemical compounds for treating air or the like
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- Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Catalysts (AREA)
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
- Physical Or Chemical Processes And Apparatus (AREA)
Abstract
Apparatus, systems and methods for forming advanced oxidation products by contacting a hydrated catalytic surface of a catalytic target structure with broad spectrum ultraviolet light in the wavelength range of 100nm to 300nm, preferably including 185nm and 254nm wavelengths. The catalytic surface reacts with the ultraviolet light energy and hydrates at the catalytic surface to form advanced oxidation products. In one embodiment, the catalytic surface comprises a hydrophilic agent, titanium dioxide, silver, copper, and rhodium. Preferably, the catalytic surface is coated with a coating comprising a hydrophilic agent, titanium dioxide, silver, copper and rhodium. A photohydrogen ionization unit (100) is also provided that includes an ultraviolet light source (204) and a catalytic target structure (110) in an air environment to form advanced oxidation products. Ultraviolet light indicators and monitoring and/or control systems for a photohydrogen ionization unit (100) are also provided.
Description
Technical Field
The present invention relates generally to the field of applying ultraviolet light to an environment to produce an oxidizing agent for killing microorganisms (e.g., bacteria, mold, and viruses) and repelling odors, and more particularly to an advanced oxidation process that utilizes ultraviolet light to provide advanced oxidation products to the environment.
Background
Oxidation is a chemical reaction in which the positive valence of an element or ion increases, losing electrons to the oxidant. Oxidation is the modification of a substance by combining it with oxygen to chemically react, for example by burning or rusting. The oxidation process can be used to kill bacteria, mold and viruses. They are also commonly used to react with odor-causing chemicals such as volatile organic compounds and other inorganic and organic chemicals.
Germicidal ultraviolet light (254nm) is used to inactivate microorganisms (e.g., germs, viruses, and bacteria). Ultraviolet light is reliable and can be easily installed. However, germicidal ultraviolet light can only effectively reduce airborne microorganisms that pass directly through the light. Unfortunately, germicidal ultraviolet light has little or no effect on gases, vapors, or odors.
While ultraviolet light energy (185nm) may produce ozone gas when applied to air in the environment and ozone is a strong oxidizer, elevated amounts of ozone may be toxic to humans and animals and may undesirably react with the environment.
Accordingly, there is a need to overcome the problems discussed above, in particular to provide an apparatus, system and method for a significantly improved oxidation process to reduce microorganisms and odors in the environment.
Disclosure of Invention
According to alternative preferred embodiments of the present invention, advanced oxidation products (e.g., hydroxyl, ozone, hydroperoxyl, ozonide, hydroxide and superoxide ions, hydrogen peroxide) may be formed by novel and novel apparatus, systems, and methods. These higher oxidation products include potent oxidants that react with undesirable compounds in the environment (e.g., microorganisms, odor-causing chemicals, and other inorganic and organic chemicals) to destroy and/or inactivate such compounds.
According to a preferred embodiment of the invention, the apparatus comprises: an ultraviolet light source for emitting ultraviolet light, the ultraviolet light emitted from the ultraviolet light source comprising ultraviolet light energy at about 100nm and at about 300 nm; and a catalytic target structure mechanically coupled to the ultraviolet light source and comprising a surface, the surface of the catalytic target structure comprising titanium dioxide and at least one of the following metal compounds: silver, copper and rhodium, and wherein the surface of the catalytic target structure reacts with hydrates at the surface after contact with ultraviolet light to form advanced oxidation products.
The catalytic surface of the catalytic target structure preferably comprises titanium dioxide, silver, copper and rhodium. Furthermore, according to an alternative preferred embodiment, the catalytic surface comprises a hydrating agent (hydrophilic compound) as well as titanium dioxide, silver, copper and rhodium. The hydrating agent may include water, moisture, and/or humidity at the catalytic surface, while the hydrophilic agent may include silica gel, calcium chloride, sodium chloride, or other known agents having hydrating properties.
According to an alternative preferred embodiment, the catalytic surface is designed for maximum surface contact with ultraviolet light. Preferably, the surface comprises a ridge or a corrugated design.
According to a preferred embodiment, the photo-hydrogen ionization unit comprises a catalytic target structure substantially surrounding the ultraviolet light source. The new and novel photohydrogen ionization unit is effective for forming advanced oxidation products for advanced oxidation processes.
According to an alternative preferred embodiment of the present invention, a system for forming advanced oxidation products comprises: at least one ultraviolet light source for emitting ultraviolet light, the ultraviolet light emitted from the at least one ultraviolet light source comprising ultraviolet light energy at about 100nm and at about 300 nm; and at least one catalytic target structure comprising a surface in contact with ultraviolet light from the at least one ultraviolet light source, the surface of the at least one catalytic target structure comprising titanium dioxide and at least one (preferably three) of the following metal compounds: silver, copper and rhodium, and wherein the surface of the at least one catalytic target structure reacts with hydrates at the surface after contact with ultraviolet light to form advanced oxidation products. In an alternative embodiment, the system includes a plurality of ultraviolet light sources and a plurality of catalytic target structures.
The novel and novel coating of the surface of the catalytic target structure preferably comprises various combinations of: hydrophilic agents, titanium dioxide, silver, copper and rhodium, such that a catalytic target surface having a coating at the surface would be useful for forming advanced oxidation products according to alternative preferred embodiments of the present invention.
According to an alternative embodiment of the present invention, a novel and novel process for forming advanced oxidation products is also provided. The method preferably comprises: hydrating a catalytic surface comprising titanium dioxide and the following metal compounds: silver, copper and rhodium; contacting the catalytic surface with ultraviolet light; and forming advanced oxidation products at the catalytic surface. The method may optionally include hydrophilically absorbing hydrates from the atmosphere surrounding the catalytic surface.
Drawings
The features and advantages of the invention will become apparent from the following detailed description of embodiments thereof, provided by way of non-limiting example only, with reference to the accompanying drawings, in which:
fig. 1 is a perspective view of a PHI unit according to a preferred embodiment of the present invention.
Fig. 2 is a perspective view of the PHI unit of fig. 1 with one side thereof partially cut away to show a portion of an internal UV light source, according to a preferred embodiment of the present invention.
FIG. 3 is a cross-sectional side view of the PHI unit of FIG. 1 showing an internal UV light source and surrounding catalytic target structure, in accordance with a preferred embodiment of the present invention.
FIG. 4 is a cross-sectional side view of an alternative PHI unit showing an internal UV light source and surrounding catalytic target structure according to an alternative preferred embodiment of the present invention.
Fig. 5 through 8 are cross-sectional side views of a portion of an exemplary PHI unit showing an advanced oxidation process that produces advanced oxidation products on the surface of a catalytic target structure and in the ambient environment, according to one embodiment of the invention.
Fig. 9 is a perspective view of an exemplary application of a PHI unit on a mounting plate according to a preferred embodiment of the present invention.
FIG. 10 is a cross-sectional side view of an exemplary Air Conditioning (AC) duct system including a PHI unit installed in the AC duct system, according to a preferred embodiment of the present invention.
FIG. 11 is a bottom view of the AC air return duct showing the PHI unit installed in the AC duct system in accordance with a preferred embodiment of the present invention. We need to include other embodiments, stand-alone units with internal air movers (fans), stand-alone units using convection.
FIG. 12 is an exemplary functional block diagram of a system utilizing a new and novel PHI unit according to an embodiment of the present invention.
Fig. 13 shows a partial structural schematic of a new and novel PHI unit in accordance with one embodiment of the present invention.
Detailed Description
As required, detailed embodiments of the present invention are disclosed herein; however, it is to be understood that the disclosed embodiments are merely exemplary of the invention, which can be embodied in various forms. Therefore, specific structural and functional details disclosed herein are not to be interpreted as limiting, but merely as a basis for the claims and as a representative basis for teaching one skilled in the art to variously employ the present invention in virtually any appropriately detailed structure. Further, the terms and phrases used herein are not intended to be limiting; but rather to provide an understandable description of the invention.
The terms "a" or "an," as used herein, are defined as one or more than one. The term "plurality", as used herein, is defined as two or more than two. The term another, as used herein, is defined as at least a second or more. The terms including and/or having, as used herein, are defined as comprising (i.e., open language).
According to alternative preferred embodiments of the present invention, the apparatus, system and method utilize advanced oxidation processes to react with compounds in the environment such as microorganisms, odor-producing chemicals and other inorganic and organic chemicals. The oxidizing agents produced during advanced oxidation processes are much more effective than traditional oxidizing agents in reacting with compounds such as microorganisms, odor-producing chemicals, and other inorganic and organic chemicals. Oxidants that can be generated during advanced oxidation are significantly stronger than typical scavengers such as chlorine. These oxidizing agents, commonly referred to as advanced oxidation products or AOPs, include ozone, hydroxyl radicals, hydrogen peroxide, ozonide ions, hydroxide and superoxide ions. All of these compounds are used during or produced as a result of the advanced oxidation process. Typically, the higher oxidation products will react with compounds that are generally unreactive with other common oxidants.
An example of one strong oxidizing agent produced by advanced oxidation processes is a hydroxyl radical. The hydroxyl group (OH-) is very unstable, making it very aggressive towards free radicals. One method of generating hydroxyl radicals or free radicals is when ozone and water react with ultraviolet light energy and proton transfer occurs. Although the hydroxyl groups have a shorter lifetime, they have a higher oxidation potential than ozone, chlorine or hydrogen peroxide, and their unstable nature increases their reaction rate. The powerful benefits of advanced oxidation are carbon dioxide and water end products.
By utilizing redundant oxidants, according to preferred embodiments of the present invention, the speed and efficiency of the oxidation process can be greatly increased, in some cases by over 40-fold. An oxidizing agent that is significantly stronger than traditional purification chemicals such as chlorine can be produced in large quantities by using a combination of oxidizing agents in a process as will be discussed below. Oxidants such as hydroxyl, ozone, hydrogen peroxide and superoxide ions may be used during or generated as a result of the advanced oxidation process. By utilizing advanced oxidation in the process, it produces reactions in the environment that provide scavenging ions, such as hydrogen peroxide and superoxide ions, which react with the surrounding atmosphere and compounds such as microorganisms or odor-producing chemicals. According to a preferred environment of the present invention, the advanced oxidation reaction process occurs when light energy from the ultraviolet light source reacts with oxygen, ozone, small amounts of moisture in the air, and the hydrated multi-metallic catalytic surface of the target structure, as will be discussed in more detail below.
According to a preferred embodiment of the present invention, the advanced oxidation process utilizes a broad spectrum ultraviolet light source comprising an ultraviolet light element targeted to the multi-metallic catalytic surface of the target structure. The surface preferably comprises a multi-metallic catalytic and hydrophilic material, which can be presented in a number of different ways, as discussed in more detail below. The hydrophilic surface attracts and absorbs moisture from the surrounding air. Preferably, a broad spectrum ultraviolet light source is used to illuminate the surface of the target structure and to provide energy to the surrounding atmosphere of the environment. The broad spectrum ultraviolet light source includes two ultraviolet light bands at a wavelength of about 254nm and at a wavelength of about 185 nm. Ultraviolet energy at 254nm is directed to the target surface and activates the production of hydroxyl radicals, superoxide ions and hydrogen peroxide on the surface. The surface is also preferably hydrophilic to absorb moisture from the ambient air in the environment. The ultraviolet light energy at a frequency of 254nm energizes the catalytic surface, causing the surface to react with water molecules in the surrounding air and primarily on the hydrophilic surface, causing them to break into hydroxyl radicals during advanced oxidation, as will be discussed in more detail below.
The broad spectrum ultraviolet light source also produces ultraviolet light energy emitted at 185 nm. The energy of the emitted photons at this wavelength is sufficient to cause the oxygen molecules to break apart to form ozone gas. These ozone molecules in the air are then reduced to oxygen via a decomposition process initiated by 254nm ultraviolet energy (providing another type of advanced oxidation reaction) also emitted from a broad spectrum ultraviolet energy source. The results from this reaction process also produce hydroxyl radicals, superoxide ions and hydrogen peroxide, similar to the surface reactions discussed previously. Using the photohydrogen ionization process, not only is the target surface active, but also the air space between the target surface and the ultraviolet light energy source.
Advantageously, this process not only uses germicidal ultraviolet light energy to treat the air in the environment, it has the added effect of: the air continues to be treated even after it leaves the surrounding area of the target surface. This process is very effective in reducing microorganisms, odors, and other chemicals in the environment. This is a clear advantage over conventional uv and advanced oxidation systems that only reduce microorganisms and compounds at the point of treatment. According to a preferred embodiment of the present invention, the advanced oxidation gas generated by the photohydrogen ionization process includes a safe and environmentally friendly oxidant that returns to oxygen and hydrogen upon reaction with contaminants. Residual ozone generated as a by-product of ozonolysis (advanced oxidation reaction) is a safe low concentration. According to a preferred embodiment of the present invention, this advantageous photohydrogen ionization (PHI) process generates ozone and reduces it to a safe low level. This process also does not require maintenance or technical intervention. The process is passive in operation and the surface of the target acts as a catalyst to produce the advanced oxidation reaction without actually affecting the target structure itself. This advanced oxidation system and process is far safer than past conventional ozone generators and much more effective in destroying microorganisms than conventional germicidal ultraviolet systems. In addition, the new and novel advanced oxidation system and process reduces environmental odors that cannot be accomplished with germicidal ultraviolet light systems. The surface of the target energized by the ultraviolet light, along with the surrounding air, produces advanced oxidation products without the production of nitric oxide gas or nitric acid, which are recognized as irritants and pollutants harmful to humans and animals (these are typically produced by other means of ozone generation). According to a preferred embodiment of the present invention, the novel and novel advanced oxidation process produces a combination of powerful oxidants such as hydrogen peroxide, oxide ions, hydroxyl radicals and superoxide ions, and also produces a redundant oxidizing gas that can be used in a variety of useful applications.
We need to mention the PPC benefits, the UV lamp and mercury insulation and leakage prevention properties. We should also include a way to change the UV outer spectrum to tune it to our desired output by using varying voltage and frequency across the lamp.
Fig. 1 and 2 illustrate a photo-hydrogen ionization (PHI) cell 100 according to a preferred embodiment of the present invention. The PHI unit 100 is an exemplary advanced oxidation reaction unit that can be used in many different applications, as will be discussed below. The PHI unit 100 includes a catalytic target structure 110 that substantially surrounds an ultraviolet light energy source (not shown in fig. 1). Preferably, the catalytic target structure 110 is also a hydrophilic structure that absorbs water molecules at the surface of the target structure, as already discussed above.
The PHI unit 100 includes a bottom cover 102 and a top cover 104 that, in combination, structurally support a source of ultraviolet energy and a surrounding catalytic target structure 110 as an integral unit. Although not shown in fig. 1 and 2, according to one exemplary embodiment, a silicon collar (or gasket) and a metal collar inside the bottom cover 102 operate in combination to secure and seal one end of the ultraviolet (u.v.) lamp 204 to the bottom cover 102, and a securing clip inside the top cover 104 secures the other end of the u.v. lamp 204 to the top cover 104. The bottom cover 102 and top cover 104 may also include features or additional structural elements, such as tabs 106, 108, for engaging and further supporting the PHI unit 100 with other structures, as will become apparent to those of ordinary skill in the art in view of the present discussion.
At the bottom cover 102 end of the PHI unit 100, a mating connector end 120 for an ultraviolet light energy source 204, such as a UV lamp 204, is shown with a mating connector 122 for providing electrical contacts for electrically coupling the ultraviolet light energy source 204 to an external power source (not shown). At the bottom cover 102, in this example, there are mechanical mating structures 130, 132 that mechanically couple the PHI unit 100 to another structure (not shown). For example, the mechanical mating structures 130, 132 may connect the PHI unit 100 to a support structure (e.g., a mounting plate) by passing threaded bolts through corresponding openings in the mechanical coupling structures 130, 132 to secure the PHI unit 100 to another structure, e.g., to secure the PHI unit 100 to a mounting plate, with locking nuts (not shown) threaded onto the threaded bolts.
The catalytic target structure 110 preferably comprises only a partially closed structure with open areas, e.g. pores 112, 114, which allow the passage of ambient gas near the catalytic target surface and also allow a portion of the ultraviolet light energy. In an exemplary embodiment, the mechanocatalytic target structure 110 has about 50% active catalytic surface, with the remaining areas being open areas, e.g., pores 112, 114, to allow ultraviolet photon energy to pass through the target structure 110, thus facilitating additional reactions outside the PHI unit 100. The target structure 110 may vary between 0% (flow cell) and 95% open area, with a preferred percentage of open area between 40% and 60% open area, as desired for different applications.
The catalytic target structure 110 is preferably shaped to allow for substantially maximum surface area while limiting the angle of incidence of the ultraviolet photon energy directed at the target structure 110. For example, the repeating V-shaped geometry in the ridge or pleat design allows for the proper ratio of open area to closed area and maximizes the surface area of the catalytic target 110 that will be exposed for reaction with the uv light energy and the surrounding environment. The repeating V-shaped structures can of course be altered or modified to other geometries to accommodate alternative manufacturing requirements, new available manufacturing techniques, textured or faceted surface impingement, circular or contoured target structures, air or fibrous materials, or any suitable structure that generally increases the available surface area for the hydrophilic catalytic material to react with the ultraviolet light energy and ambient gases. The structure of the PHI unit 100 may also vary from the preferred embodiment to meet specific structural requirements due to the particular application, as should be apparent to one of ordinary skill in the art in view of the present discussion. For example, a large or customized PHI unit may have different structural requirements in a particular application.
With continued reference to fig. 1 and with reference to fig. 2, the internal ultraviolet energy source 204 is exposed in the cross-sectional view of fig. 2 with a portion of the catalytic target structure 110 and the top cover 104 removed. The uv energy source 204 (a uv lamp in this example) includes a sealing cap 206 at the top end of the lamp 204. The UV lamp 204 is shown extending outwardly from the catalytic target structure 110 at the cut-out end 202. However, in a preferred arrangement, the UV light source 204 is substantially surrounded by the catalytic target structure 110 to substantially maximize the surface area of the catalytic target structure 110 exposed to the ultraviolet light energy from the u.v. lamp 204. In this example, the catalytic target structure 10 generally surrounds the ultraviolet light energy source 204 radially along the central axis of the UV lamp 204. This preferably provides maximum catalytic surface contact to available u.v. photonic energy. The broad spectrum UV light source 204 is preferably designed to operate in a wavelength range of between approximately 100 to 300nm (always including a band of wavelengths of approximately 185nm and 254 nm). The UV light source 204 may be a low pressure mercury vapor lamp (typical standard HO or VHO output), a medium pressure mercury vapor lamp, or LED based technology (or any combination of these).
Although in this example the catalytic target structure 110 radially surrounds the UV lamp 204, when using LED-based technology, the LED array may be arranged radially or on a planar axis with respect to the catalytic target structure, with the intention that the catalytic target structure conforms to the overall shape of the LED array to allow maximum catalytic surface exposure to the UV light source. Other arrangements between the at least one u.v. light source and the surface of the catalytic target structure are contemplated based on the present discussion, according to design choice for alternative applications, as should be apparent to one of ordinary skill in the art in view of the present discussion. For example, the at least one u.v. light source and preferably a plurality of u.v. light sources may be positioned in relatively close proximity to at least one surface of at least one application-specific catalytic target structure in an environment, wherein the surface of each application-specific catalytic target structure may be specifically shaped and adapted to provide a desired utility in a particular application while also providing a catalytic target surface for enhancing the formation of advanced oxidation products at the surface of such application-specific catalytic target structure.
As a more detailed, non-limiting example, a plurality of wide-spectrum u.v. lamps may be located within an air-handling duct system, wherein the interior surface of the duct (or ducts) substantially surrounding the plurality of wide-spectrum u.v. lamps includes a catalytic target structural material that is substantially in contact with the u.v. photon energy from the u.v. lamps to promote the formation of advanced oxidation product reactions at such surfaces. Of course, each such u.v. lamp may additionally be radially surrounded by the catalytic target structure 110, as already discussed above, to additionally promote the formation of advanced oxidation product reactions at the surface of the catalytic target structure 110. As another alternative example of utilizing multiple u.v. light sources, wherein at least one u.v. light source is substantially surrounded by a catalytic target structure 110, the outer surface of each such catalytic target structure 110 may be exposed to the u.v. light of a u.v. lamp external to and proximate to the particular catalytic target structure 110, thereby additionally promoting the formation of advanced oxidation product reactions at the outer surface of the particular catalytic target structure 110. Typically, it will enhance the advanced oxidation product formation process accordingly by contacting a large available exposed surface area of the at least one catalytic target structure and, depending on the particular application, the plurality of catalytic target structures with u.v. photonic energy.
The catalytic target structure material includes a variety of compounds, particularly at the surface of the catalytic target structure 110. Preferably, the catalytic target surface material comprises five compounds, i.e., four metal compounds and a hydrating agent. These compounds preferably include titanium dioxide (TiO)2) Copper metal (Cu), silver metal (Ag), rhodium (Rh), and a hydrating agent (e.g., silica gel (tetraalkoxysilane TMOS, tetramethoxysilane, tetraethoxysilane TEOS)). Hydrating agents may also comprise any suitable compound having an affinity to attract or absorb surrounding waterOr a combination of compounds (i.e., hydrophilic and hydrating agents). The combination of the various metal compounds identified above, and preferably the combination of four metal compounds, at the surface of the catalytic target structure 110 includes a novel and novel structure for the advanced oxidation process to produce an advanced oxidation product reaction, as discussed in more detail below.
Silver has antimicrobial properties. For example, if air hits the silver at the surface of the catalytic target 110, it kills microorganisms in the air. It has been found that titanium dioxide combined with silver at the surface of the catalytic target 110 (as compared to using titanium dioxide alone without silver) can lead to the formation of higher oxidation product reactions (e.g., the formation of hydroxyl groups, superoxide ions, and hydrogen peroxide) approximately 3 times faster. Copper has antimicrobial properties and also helps to accelerate the reaction at the surface of the catalytic target structure 110 to produce advanced oxidation products. Rhodium has antimicrobial properties and is also a catalyst that destroys nitrogen compounds and enhances the formation of higher oxidation products.
The hydrate compound significantly increases the formation of higher oxidation product reactions, primarily hydroxyl products on the surface of the catalytic target structure 110 and within the environment surrounding the catalytic target 110. The ambient humidity in the environment surrounding the catalytic target 110 and the induced humidity (via forced evaporation, ultrasonic atomization, or other suitable means) typically provide humidity at the surface of the catalytic target 110, providing a hydrating agent (i.e., water) at the surface of the catalytic target 110 to promote the formation of advanced oxidation product reactions. Furthermore, ambient humidity as well as induced humidity may be attracted to the catalytic target surface by hydrophilic and hydrating compounds, such as silica gel, at the surface of the catalytic target 110 to significantly enhance the formation of advanced oxidation product reactions at the surface of the catalytic target 110. This is a particularly significant advantage of the present invention.
The combination of the five compounds discussed above may vary from less than 1% to more than 90% of any of the five compounds, as may be desired for different applications according to alternative embodiments of the present invention. Different fabrication techniques and methods may be used to provide the surface of the catalytic target structure 110 with a combination of desired compounds as discussed above. For example, a coating comprising a desired compound may be provided to the surface of the catalytic target structure 110. These various manufacturing techniques and methods may include, but are not limited to, adhesives, polymers, baking (low and high heat applications), charging, and pigment carrier technologies. In addition, other non-specific compounds may be added to the combination of the five compounds to aid in adhesion and/or adherence to any particular surface of the catalytic target structure 110, as will become apparent to those of ordinary skill in the art in view of the present discussion.
According to one non-limiting example, a combination of the preferred five compounds may be provided in a mixture that also includes a base solvent to provide a mixed solution. The mixed solution may then be deposited onto the surface of the catalytic target structure 110, for example by spraying or by other known deposition methods. The base solvent will then evaporate, leaving the desired combination of compounds at the surface of the catalytic target structure 110. The method used to provide the combination of desired compounds to the surface of the catalytic target structure 110 will depend entirely on the design choice of the commercially available technology used to make the particular target structure useful in the application.
Referring to fig. 3, a cross-sectional side view of an exemplary PHI unit 100 is shown, in accordance with a preferred embodiment of the present invention. The inner UV lamp 204 is substantially surrounded by the outer catalytic target structure 110. In this example, the UV lamp 204 contains mercury vapor gas 302 that when energized at the appropriate frequency (e.g., by electrical energy provided through electrical contacts of the mating connector 122) will produce a broad spectrum of ultraviolet light energy radiated from the UV lamp 204. The UV lamp 204 has an outer surface that is preferably substantially coated with a protective barrier coating, in this example a fluorocarbon protective coating or film 208, that substantially encases the UV light source 204 and is made of a material that allows UV light to substantially pass through the protective barrier coating, such as a preferred fluorocarbon or other protective plastic coating or barrier material. The primary purpose of this outer protective barrier coating or film structure 208 is to provide an insulating barrier to the UV light source, thereby preventing heat loss in cold operating environments, reducing temperature shock, and thus optimizing UV light source efficiency. This outer protective coating structure 208 also acts as a physical barrier (leak-proof barrier) that prevents quartz, glass, mercury, or other materials used in the construction of the UV light source 204 from leaving the fluorocarbon protective barrier coating 208, i.e., in the event of accidental damage or breakage to the PHI unit 100. Another significant benefit of this fluorocarbon coating or thin film structure 208 is that it prevents debris and other contaminants from contacting and possibly adhering to the UV light source 204 and possibly reducing its operating efficiency or more importantly physically damaging it. Preferably, the protective barrier coating 208 is comprised of a fluorocarbon that provides an external non-polar surface that does not attract external contaminants or foulants, thus providing an anti-fouling protective barrier surface for the UV light source 204. This new and novel structure and arrangement allows all of the u.v. light energy from the UV light source 204 to be emitted from the protective barrier coating 208. In this example, the protective coating structure 208 may be a shrink-wrap type film or coating structure at the outer surface of the UV lamp 204. However, other protective and/or coating structures may be used at the inner and/or outer surfaces of the u.v. lamp 204, as should be apparent to one of ordinary skill in the art in view of the present discussion. Further, the material, shape, and texture of the coating structure may be changed from the fluorocarbon shrink tube of the current example to alternative materials, shapes, and textures as long as the alternative coating materials, shapes, and textures allow u.v. light to pass through the alternative coating structure such that the u.v. photon energy may contact the surface of the catalytic target structure 110 to promote advanced oxidation product formation reactions at the surface of the catalytic target structure 110.
The catalytic target structure 110 includes an inner surface 304 and an outer surface 306. The inner surface 304 is directly exposed to the inner UV lamp 204. The inner surface 304 receives ultraviolet light energy directly from the UV lamp 204. The outer surface 306 is also preferably coated with a catalytic material so that it may be exposed to ultraviolet light energy from an external ultraviolet light source or possibly reflected ultraviolet light from the internal UV lamp 204, i.e., u.v. light reflected from an external reflective surface (not shown). In particular, this reflected UV light may originate from the UV lamp 204, then pass through the openings 112, 114 (see fig. 1) of the catalysis target structure 110, and then reflect from the external structure back to the outer surface 306. In this manner, the catalytic target structure 110 substantially maximizes the exposed surface area to substantially maximize the advanced oxidation product formation reactions at the surfaces 304, 206 and in the ambient gas environment.
Referring to fig. 4, an alternative arrangement 400 of the PHI unit is shown, according to a preferred embodiment of the present invention. This alternative PHI unit 400 includes a variation of the internal UV light source such that the UV lamp 204 is surrounded by a barrier structure 402, the barrier structure 402 being sufficiently transparent to the u.v. light emitted from the u.v. lamp 204 to allow the u.v. light to pass through the barrier structure 402 and contact the surface 304 to promote the formation of advanced oxidation product reactions at the surface 304. Preferably, the barrier structure 402 is located in close proximity 404 to the outer surface of the UV lamp 204. In this alternative embodiment, the surrounding barrier structure 402 comprises a transparent tube made of a material (e.g., quartz) that is sufficiently transparent to ultraviolet light energy near the frequency of interest (i.e., about 100 to 300nm wavelength). This outer barrier structure 402 substantially surrounds and encases the inner UV lamp 204 throughout the length of the UV lamp 204. In this example, the surfaces of outer barrier tube 402 and inner UV lamp 204 are in close proximity 404 (at a nominal distance), and preferably a silicon or teflon seal creates an adhesive seal between the end of barrier tube 402 and the end of inner UV lamp 204. This outer tube 402 provides a leak-proof barrier in the event that the inner UV lamp 204 fails (e.g., to contain mercury vapor 302 and any broken glass and debris from the failed u.v. lamp 204), and also provides the benefit of thermal protection of the UV lamp 204, thereby significantly extending the usable life of the ultraviolet light energy source 204 and maximizing output efficiency by thermally stabilizing the light energy source 204, as well as protecting the light energy source 204 from wet environments (condensation in cold environments, etc.).
In general, the design and placement of the catalytic target preferably considers 1) the distance from the UV light source and 2) how to maximize the exposed surface area of the catalytic target to enhance the formation of advanced oxidation products. The closer the catalytic target is to the UV light source, the higher the UV light photon energy is provided to the surface area of the catalytic target. Furthermore, the exposed surface area of the target should be maximized to allow for the maximum surface area in contact with the u.v. photon energy and the surrounding environment for maximizing the reaction that forms and activates the advanced oxidation products. Preferably, the catalytic target comprises a ridge or corrugation design to maximize the surface area exposed to the UV light photon energy and the surrounding environment.
Referring to fig. 5, 6, 7 and 8, the formation of the advanced oxidation product process is discussed in more detail below. According to an exemplary embodiment of the invention, ultraviolet light energy from the u.v. light source 204 is emitted and directed to the surface area of the catalytic target structure 110, as already discussed above and as shown in fig. 5. The ultraviolet light energy includes a frequency at a wavelength 502 of about 185nm that interacts with oxygen 504 in the environment to produce ozone 602, as shown in fig. 6. Ozone is a strong oxidizing agent that can kill microorganisms (e.g., bacteria, molds, viruses) and also react with chemicals in the environment to reduce odors. While the UV light source 204 emitting 185nm UV light energy also emits UV light energy at a wavelength 702 of about 254nm, as shown in FIG. 7. This UV light energy at 254nm decomposes ozone back to oxygen (704), thereby also advantageously releasing hydroxyl groups and other higher oxidation products. In addition, the u.v. light energy at 254nm 702 contacts the surface of the catalytic target structure 110. The catalytic target structure 110 comprises a hydrating agent, which preferably also comprises a hydrophilic agent, attracting moisture from the air in the surrounding environment to the surface of the catalytic target structure 110. The u.v. light energy at 254nm 702 in contact with the surface of the catalytic target structure 110 reacts with the collection of water molecules and metals at the surface to produce higher oxidation products, such as hydroxyl, hydrogen peroxide, superoxide ions, which are highly reactive and will react with the surrounding environment to kill microorganisms, reduce odor, and will react with and destroy other undesirable organic and inorganic chemicals found in the environment. This results in a purification and purification process of the ambient air of the environment. These higher oxidation products are very short lived and highly reactive, such that after reaction with compounds in the environment, the higher oxidation products will (in a short time) revert to safe and harmless oxygen and water molecules. Furthermore, the ozone generated in the process will rapidly decompose and revert to oxygen (704), so that after the advanced oxidation process decontaminates the environment of microorganisms, odors, and other undesirable compounds and impurities, the ozone level in the environment is typically kept at a safe low level immediately. Furthermore, the u.v. light energy at a wavelength of 254nm exhibits bactericidal properties and beneficially kills bacteria and microorganisms that are in direct contact with the UV light energy. This also helps to kill microorganisms in the surrounding air and in the environment. Additional wavelengths from 100 to 300nm are also utilized to react with the compound using activation energy corresponding to different wavelengths of the UV light source 204.
FIG. 8 illustrates a general exemplary advanced oxidation product formation process according to a preferred embodiment of the present invention. The broad spectrum u.v. light energy 802 from the u.v. light source 204 interacts with the surrounding environment and contacts the surface of the catalytic target structure 110. In this example, the 185nm wavelength from the broad spectrum u.v. light source 204 substantially generates ozone, and substantially simultaneously destroys ozone at the 254nm wavelength and converts it to oxygen. The combination of ozone generation and destruction in the atmosphere of the environment surrounding the u.v. light source 204 and the reaction at the surface of the hydration catalytic target structure 110 produce the multiple benefits of germicidal u.v. light, hydroxyl radicals, superoxide ions, hydrogen peroxide, oxide ions and peroxides, and other such advanced oxidation products. The combination of the surface of the advanced oxidation products and the germicidal u.v. light simultaneously provides the benefits of significant microbial reduction, reduced odor, and removal of certain undesirable chemicals in the environment. For example, the advanced oxidation process kills out as follows: paint, pet odors, sewer odors, volatile organic compounds, chemical odors, sanitizing chemical odors, cooking odors, rotting organic matter, viruses, fire and smoke, garbage odors, hydrocarbons, mold and mildew, and other microorganisms.
Reference is made to fig. 9, 10 and 11, which illustrate an exemplary application of the new and novel advanced oxidation process according to one of the preferred embodiments of the present invention. A system for purifying and decontaminating air conditioning and/or heating (AC) ductwork is shown that utilizes a novel and novel advanced oxidation process to eliminate the risk of sick building syndrome by, for example, reducing odors, air pollutants, chemical odors, smoke, mold, bacteria, and viruses. As shown in fig. 9, the PHI unit 100 is mounted at its bottom cover 102 to a mounting plate 803, the mounting plate 803 providing structural support to the PHI unit 100 when located within an AC duct 904 (see fig. 10). On the opposite side of the mounting plate 803 is shown a housing 804 containing circuitry for powering the PHI unit 100 and controlling the PHI unit 100. The housing 804 includes, for example, a power supply and ballast circuitry for powering the PHI unit 100. Further, in accordance with an alternative embodiment of the present invention, a fiber optic cable 806 extends from the PHI unit 100 through the mounting plate 803 and the housing 804 to provide an optical indicator that indicates when the PHI unit 100 is in use. This fiber optic indicator 806 may be used by the monitoring system to detect fault conditions, such as when the PHI unit 100 is not functioning properly and may require replacement of the u.v. lamp 204. In addition, the fiber optic light indicator 806 may provide a means to monitor and control the operation of the PHI unit 100 under various applications. One end of the fiber optic cable 806 is preferably in substantial contact with the broad spectrum ultraviolet light emitted from the u.v. light source 204 of the PHI unit 100, while the other end of the fiber optic cable 806 preferably emits visible light as an indication that the u.v. light source 204 in the PHI unit 100 is operational. The fiber optic cable material can provide a filtering effect for u.v. light transmitted through the fiber optic cable such that the emitted light from the fiber optic cable indicator 806 is much in the visible range and safe for use by most equipment and applications. Optionally, a filter (not shown) may be inserted at any point between the u.v. light from the PHI unit 100 and the output of the fiber optic cable indicator 806, such that the filter will substantially remove unwanted u.v. light energy (e.g., at unwanted frequencies) while allowing light in the visible range to be emitted from the fiber optic cable indicator 806. In summary, a fiber optic cable 806 (any suitable type may be used) provides a means of remotely monitoring the status of the PHI unit 100. As a security feature, the cable itself or a second filter is used to absorb wavelengths from 100 to 300nm, while allowing the visible light portion (typically in the 500nm range) to be transmitted out of the fiber optic cable to be used at a remote display point where the status of the PHI unit 100 can be directly indicated. Alternatively, the optical fiber may be made of any suitable material that transmits UV light (100-. Furthermore, this photodetector and sensor may be coupled to a variable frequency, variable voltage power supply (not shown) to energize the u.v. lamp 204, such that it may then be used to adjust and vary the overall output power (photon energy) of the u.v. lamp and the frequency-specific output energy within one or more ranges of u.v. lamp frequencies. This is a valuable feature of the preferred embodiment of the invention.
Referring to fig. 12, for example, an exemplary functional block diagram of a system 1200 utilizing the new and novel PHI unit 100 will be discussed. The system 1200 includes at least one PHI unit 1202 that includes a fiber optic cable 1204 that carries at its output an optical signal, for example, indicative of the u.v. lamp operating status of the respective PHI unit 1202.
According to a preferred embodiment of the present invention, the visible light emitted from the fiber optic cable 1204 will serve as a direct mechanical indicator of the operational status of the at least one PHI unit 1202. The fiber optic elements directly coupled to the UV source 204 in the PHI unit 100 (see fig. 1) would preferably be equipped with UV filtering characteristics, or alternatively add a separate UV filter (not shown) that could be used to transmit the visible light (typically in the range of 400 to 500 nm) emitted from the PHI unit 1202 to a remote location or unit panel to monitor the PHI unit status. Examples of these two types of installation may be: a display panel on a piece of equipment, or an indicator remotely mounted (e.g., as required in some HVAC system installations) from the PHI unit. Light transmitted along the fiber optic cable 1204 will terminate in a lens (not shown) that will illuminate and act as a visual display (not shown) for operator monitoring or other device monitoring.
For example, a photodetector or photometer (not shown) coupled to the computer system 1208 may be used to automatically monitor the ON/OFF state of at least one of the PHI units 1202. The computer system 1208, upon detecting a fault condition, such as when at least one PHI unit 1202 should be ON but detects it OFF at the photodetector or photometer (e.g., no UV light is detected or UV light is not detected above a predetermined power level), may then send an alarm signal to a user and/or operator and/or technician (which may also be referred to herein as a user/operator/technician). The alarm signal may include an audible signal (e.g., by an audible alarm sound), a visual signal (e.g., by a light on a console display or by a light source at a location readily visible to the user/operator/technician), and may even include a data signal (e.g., an email message) sent to a remote computer (not shown), or even a wireless transmission signal sent to a human portable unit (not shown), such as a cellular telephone or paging device, then the user/operator/technician may be alerted to the monitored fault condition even if the user/operator/technician is remote from the particular installation of the at least one PHI unit 1202 at the facility.
With continued reference to fig. 12, in accordance with another preferred embodiment of the present invention, the system 1200 may use UV transparent fiber optic material (e.g., quartz) in the fiber optic cable 1204 as a means of transmitting the actual UV light waves generated by the UV lamp 204 (see fig. 1). Thus, a fiber optic cable 1204 equipped with a UV transparent fiber optic material (e.g., quartz) is preferably mechanically coupled directly to the UV lamp 204 (without air space) to collect the entire 100-300nm range of UV light emitted by the UV source 204, thereby transmitting the UV light (through optical coupling) from the at least one PHI unit 1202 to the UV light detector 1206, and then the UV light detector 1206 will analyze the UV spectrum emitted from the UV lamp 204 for each of the at least one PHI unit 1202. According to this alternative embodiment, UV photodetector 1206 comprises a photometer or other spectroscopic analysis device that provides output to a user/operator/technician through a user interface (e.g., via a display (not shown)). This would enable the user/operator/technician to directly monitor and quantify the actual UV wavelength and energy output of the at least one PHI unit 1202. This may be done locally to the installation of the at least one PHI unit 1202, or may be done remotely, such as by transmitting the UV light signal through a fiber optic cable 1204 to a remotely located UV photodetector 1206.
According to another alternative embodiment of the present invention, the same method as described above may be used with the addition of a computer control system 1208 coupled to the UV photodetector 1206. According to this alternative embodiment, the UV photodetector 1206 comprises a photometer or other spectroscopic analysis device that provides output data signals indicative of the operational status of the at least one PHI unit 1202. The controller 1208 may monitor the data signals from the UV photodetector 1206 to determine a fault condition, such as an OFF state detected for any of the at least one PHI unit 1202, or an out-of-normal-operation-tolerance condition, for any of the at least one PHI unit 1202, for example. The data signals collected from the UV light detector 1206 may then be used to adjust an adjustable power supply 1210 that provides power to the at least one PHI unit 1202. The computer control system 1208 can provide output signals to a user interface. Information is then provided to a user/operator/technician who may then instruct the computer control system 1208 how to adjust the power output of the at least one PHI unit 1202. Optionally, the computer control system 1208 may automatically adjust the power output of the at least one PHI unit 1202. Additionally, the computer system 1208 may monitor the condition of at least one PHI unit 1202 and may then send information/alert signals to a user and/or operator and/or technician (which may also be referred to herein as a user/operator/technician). The information/alarm signal may comprise an acoustic signal (e.g. by an audible sound), a visual signal (e.g. by at least one light on a display or by at least one light source at a location easily visible to the user/operator/technician), and may even comprise a data signal (e.g. an email message) sent to a remote computer (not shown). The information/alarm signals may even include wireless transmission signals sent to a human portable unit (not shown), such as a cellular telephone or paging device, then the user/operator/technician may be notified/alerted of the monitored condition even if the user/operator/technician is remote from the particular installation of the at least one PHI unit 1202 at the facility. Alternative monitoring system configurations and operations should be apparent to one of ordinary skill in the art in view of this discussion.
The adjustable power supply 1210 can be adjusted to vary at least one of a frequency, a current, and a voltage of an output power signal coupled to each of the at least one PHI unit 1202. By adjusting the adjustable power supply 1210, the output electrical power signal, e.g., its voltage level or its AC frequency, is varied and then transmitted to the at least one PHI unit 1202. This will enable a user/operator/technician, or the automation controller 1208, or both, to control the operation of the at least one PHI unit 1202. For example, the user/operator/technician or the automatic controller 1208 may "dial in" (adjust) the adjustable electrical power signal to adjust the u.v. source output of the at least one PHI unit 1202, such as the total output power or, for example, the output power level of one or more frequency ranges that meet a particular output energy profile, according to the requirements of a particular application or to ensure that an optimal output of the at least one PHI 1202 is achieved during its operating life.
Referring again to fig. 9, 10 and 11, an exemplary system and application of the new and novel PHI unit 100 is shown and will be discussed below. As shown in fig. 9 and 10, the PHI unit 100 and mounting plate 803 are arranged and mounted to the AC duct 904 in a mounting arrangement 902 such that air passing through the AC duct 904 flows through and contacts the PHI unit 100. As shown in fig. 10, the PHI unit 100 extends generally within the AC duct 904 through an opening in one of the walls of the AC duct 904 and is supported where appropriate by a mounting plate 803 (shown in fig. 9) and an external housing 804 that includes circuitry to power the PHI unit 100 and control the PHI unit 100. The housing 804 may also be remotely mounted to allow installation in areas where sufficient space is not available.
The air inlet 906 receives air from the building environment including contaminants, odors, mold, bacteria, viruses, and other undesirable chemicals. As this air passes through the duct 904, it comes into contact with and is exposed to the PHI unit 100 and u.v. light, and as has been discussed earlier, the advanced oxidation process will substantially purify and purify the air. This air is then driven through the remaining AC duct 904 and combined with the high-level oxidation products produced in the PHI unit, where it continues to reduce residual contaminants as the remaining high-level oxidation products produced in the PHI unit travel down the duct with the air. Any remaining advanced oxidation products then exit and enter the room where they continue to rapidly reduce any additional ambient contaminants encountered. In addition, the germicidal UV light helps to destroy microorganisms, such as germs, molds, viruses, and bacteria, passing through the a.c. pipe 904. In this manner, the advanced oxidation process provided by the PHI unit 100 in this application is combined with germicidal u.v. light to purify and purify air for use in a building environment.
According to another alternative embodiment of the present invention, the PHI unit 100 is intended to function as a modular system that can be used singly or multiply (limited only by the particular application). The PHI unit 100 itself may be adapted to conform to various types of installations. In one embodiment, the PHI unit 100 is installed via an attached plate to facilitate handling in many different types of installations, such as in an HVAC system (e.g., in an AC ductwork system as already discussed above). In yet another embodiment, the PHI unit 100 is attached to a rigid structure (sometimes with a fan assembly) via flexible clips to facilitate air handling in multiple applications.
In one embodiment, utilizing the novel superhydrophilic photocatalytic coating in combination with active ionization, the photohydrogen ionization (PHI) process is a unique air and surface treatment system that greatly reduces airborne microorganisms, VOCs, and particulates.
The PHI technique uses a broad spectrum UV emitter (this may be a LED for mercury vapor technology) ideally in the 100-400nm spectrum. This UV energy is in turn used to activate the unique photocatalyst coated on the folded and perforated longitudinal cell structure. This energy in turn activates the photocatalyst to produce advanced oxidation reactions on the surface and in the interlamellar spaces of the PHI unit. A unique catalyst comprises an extremely porous anhydrous magnesium carbonate substrate interspersed with in-situ formed titanium dioxide crystals (anatase structure). This catalyst substrate may also include a cerium oxide reinforcing structure with additional photoreaction enhancers (including silver, zinc, rhodium, and copper metals). The anhydrous nature and the extremely porous nature of the catalyst create an affinity to promote maximum water absorption, allowing it to capture water vapor very efficiently from the surrounding air. The titanium dioxide portion of the matrix is continuously photo-activated by multiple wavelengths of UV light, which causes the captured water and air that produces superoxide ions, hydroxyl radicals, and some ozonide ions to undergo a high-level oxidation reaction (this reaction produces hydrogen peroxide that is released from the unit structure). Furthermore, VOC and microorganisms in contact with the light activated structure can also be reduced directly by such direct contact with the coating. However, the main purpose of this part of the unit is the collection of water vapour, and its subsequent conversion to hydroperoxides (mainly hydrogen peroxide vapour), and the subsequent continuous release of these hydrogen peroxides to the treatment space. This released vapor (sometimes referred to as plasma) travels outside the unit and continues by means of an integrated fan or HVAC system present in the treated building in some cases. This activated air may also help to clean the HVAC ducting as it travels through the HVAC ducting, and it is then eventually released into the interior ambient air of the building or facility being treated. Here, hydrogen peroxide can react with both airborne and surface contaminants (making it an extremely unique and efficient treatment system).
Reference is made to fig. 13, which is a schematic diagram of a portion of the structure of a new and novel PHI unit in accordance with one embodiment of the present invention. The foregoing process is further enhanced by the activation of positive and negative ions released from the high frequency bipolar ionizer 1301 of the PHI unit, which react with contaminants and PHI products. Another advantage of ion enhancement is that it has an aggregating effect on the fine charged particles (airborne particles) in the air. This allows the unit to also help control and reduce PM2.5 pollutants. These very fine particles are effectively allowed to separate from the air column by agglomeration and by greatly enhancing conventional active filtration.
The designed ion distribution technology is further enhanced by the integrated automatic self-cleaning capability of the ion emitter. Due to their charged nature, these emitters can collect charged particles over time, which if allowed to continue collecting can cause a significant reduction in the concentration of the emitted ions. The PHI unit utilizes two carbon fiber ion emitters 1303 and 1303 'mounted directly to a self-cleaning oscillating tuning fork 1302, the tuning fork 1302 directly causing mechanical oscillation of the carbon fiber ion emitters 1303 and 1303' when activated by a high frequency vibration motor 1304, effectively shaking them to clean at pre-programmed intervals.
The advanced oxidation process provided by alternative embodiments of the present invention as discussed above includes reaction with any combination of hydroxyl groups, superoxide ions, hydrogen peroxide, ozonide ions and hydroxides, and other such advanced oxidation products, which revert to oxygen and hydrogen after oxidation of the contaminants. Furthermore, in certain alternative embodiments, germicidal UV light may additionally help to destroy microorganisms, such as germs, molds, viruses, and bacteria. In this way, the advanced oxidation process and optionally in combination with germicidal u.v. light decontaminates and purifies the environment by reducing microorganisms, odors, and other undesirable chemicals in the environment. The advanced oxidation process as provided by the alternative embodiments of the present invention may be very useful in many different applications, as should be apparent to one of ordinary skill in the art in view of the above discussion.
While there has been shown and described what are at present considered to be the preferred embodiments of the invention, it will be understood by those skilled in the art that various other modifications may be made, and equivalents may be substituted, without departing from the true scope of the invention. In addition, many modifications may be made to adapt a particular situation to the teachings of the present invention without departing from the central inventive concept described herein. Moreover, embodiments of the invention may not include all of the features described above. Therefore, it is intended that the invention not be limited to the particular embodiment disclosed, but that the invention will include all embodiments falling within the scope of the appended claims.
Claims (49)
1. An apparatus for forming advanced oxidation products, the apparatus comprising:
an ultraviolet light source for emitting a broad spectrum of ultraviolet light having a wavelength between 100nm and 300nm, the emission of the ultraviolet light from the ultraviolet light source comprising ultraviolet light energy at 185nm and at 254 nm; and
a catalytic target structure mechanically coupled to the ultraviolet light source and comprising a surface, the surface of the catalytic target structure comprising titanium dioxide and at least one of the following metal compounds:
silver;
zinc;
copper; and
(ii) rhodium (II),
wherein the titanium dioxide is formed in an anhydrous magnesium carbonate substrate, at least one of the metal compounds is contained in a cerium oxide reinforced structure having an additional photoreaction enhancer,
and wherein the surface of the catalytic target structure reacts with hydrates at the surface to form advanced oxidation products after contact with ultraviolet light.
2. The apparatus of claim 1, wherein the surface of the catalytic target structure comprises titanium dioxide and a plurality of the following metal compounds:
silver;
zinc;
copper; and
and rhodium.
3. The apparatus of claim 1, wherein the surface of the catalytic target structure comprises titanium dioxide, silver, zinc, copper, and rhodium.
4. The apparatus of claim 3, wherein the surface of the catalytic target structure comprises a hydrophilic agent.
5. The apparatus of claim 4, wherein the hydrophilic agent comprises silica gel.
6. The apparatus of claim 1, wherein the surface of the catalytic target structure comprises a hydrophilic agent.
7. The apparatus of claim 6, wherein the hydrophilic agent comprises silica gel.
8. The apparatus of claim 1, wherein the surface of the catalytic target structure is hydrated by a hydrating agent at the surface, and wherein the surface reacts with hydrates from the hydrating agent at the surface to form advanced oxidation products after contact with ultraviolet light.
9. The apparatus of claim 8, wherein the hydrating agent comprises water at the surface of the catalytic target structure.
10. The apparatus of claim 8, wherein the hydrating agent comprises at least one of moisture and humidity at the surface of the catalytic target structure.
11. The apparatus of claim 8, wherein the hydrating agent comprises a hydrophilic agent at the surface of the catalytic target structure.
12. The apparatus of claim 11, wherein the hydrophilic agent comprises silica gel.
13. The apparatus of claim 1, wherein the surface of the catalytic target structure is coated with a coating comprising titanium dioxide and at least one of the following metal compounds:
silver;
zinc;
copper; and
(ii) rhodium (II),
wherein the titanium dioxide is formed in an anhydrous magnesium carbonate substrate, at least one of the metal compounds is contained in a cerium oxide reinforced structure having an additional photoreaction enhancer,
and wherein the surface reacts with hydrates at the surface to form advanced oxidation products after contact with ultraviolet light.
14. The apparatus of claim 13, wherein the coating comprises titanium dioxide and a plurality of the following metal compounds:
silver;
zinc;
copper; and
and rhodium.
15. The apparatus of claim 13, wherein the coating comprises titanium dioxide, silver, zinc, copper, and rhodium.
16. The apparatus of claim 13, wherein the coating further comprises a hydrophilic agent.
17. The apparatus of claim 16, wherein the hydrophilic agent comprises silica gel.
18. The apparatus of claim 1, further comprising an ionizer for releasing positive ions and negative ions.
19. The apparatus of claim 18, further comprising an ion emitter having integrated automatic purging capability.
20. The apparatus of claim 19, wherein the ion emitter is a carbon fiber ion emitter.
21. A mixture of compounds for providing a coating for catalyzing the surface of a target structure, the mixture comprising titanium dioxide and at least one of the following compounds: silver, zinc, copper and rhodium, the titanium dioxide being formed in an anhydrous magnesium carbonate substrate, at least one of the compounds being contained in a cerium oxide reinforced structure having an additional photo-reaction enhancer, and wherein the coating at the surface of the catalytic target structure is in reactive contact with ultraviolet light and hydrates to form advanced oxidation products.
22. A mixture of compounds for providing a coating for catalyzing a surface of a target structure, the mixture comprising a hydrophilic agent and at least one of the following compounds: titanium dioxide, silver, zinc, copper and rhodium, at least one of said compounds being formed in an anhydrous magnesium carbonate substrate, at least one of said compounds being contained in a ceria-reinforced structure with an additional photo-reaction enhancer, and wherein said coating at said surface of the catalytic target structure is reactively contacted with ultraviolet light and hydrates to form advanced oxidation products.
23. The mixture of claim 22, wherein the mixture comprises the hydrophilic agent and titanium dioxide, silver, zinc, copper, and rhodium.
24. A system for forming advanced oxidation products, the system comprising:
at least one ultraviolet light source for emitting a broad spectrum of ultraviolet light in the range of 100nm to 300nm, the ultraviolet light emitted from the at least one ultraviolet light source comprising ultraviolet light energy at 185nm and at 254 nm; and
at least one catalytic target structure comprising a surface in contact with ultraviolet light from the at least one ultraviolet light source, the surface of the at least one catalytic target structure comprising titanium dioxide and at least one of the following metal compounds:
silver;
zinc;
copper; and
(ii) rhodium (II),
wherein the titanium dioxide is formed in an anhydrous magnesium carbonate substrate, at least one of the metal compounds is contained in a cerium oxide reinforced structure having an additional photoreaction enhancer,
and wherein the surface of the at least one catalytic target structure reacts with hydrates at the surface to form advanced oxidation products after contact with ultraviolet light.
25. The system of claim 24, wherein the surface of the at least one catalytic target structure is coated with a coating comprising titanium dioxide and at least one of the following metal compounds:
silver;
zinc;
copper; and
and rhodium.
26. The system of claim 24, wherein the surface of the at least one catalytic target structure is coated with a coating comprising a hydrophilic agent, titanium dioxide, silver, zinc, copper, and rhodium.
27. The system of claim 24, comprising:
a plurality of ultraviolet light sources for emitting a broad spectrum of ultraviolet light in the range of 100nm to 300nm, the ultraviolet light emitted from at least one of the plurality of ultraviolet light sources comprising ultraviolet light energy at 185nm and at 254 nm; and
at least one catalytic target structure comprising a surface in contact with ultraviolet light from the plurality of ultraviolet light sources, the surface of the at least one catalytic target structure comprising titanium dioxide and at least one of the following metal compounds:
silver;
zinc;
copper; and
(ii) rhodium (II),
wherein the titanium dioxide is formed in an anhydrous magnesium carbonate substrate, at least one of the metal compounds is contained in a cerium oxide reinforced structure having an additional photoreaction enhancer,
and wherein the surface of the at least one catalytic target structure reacts with hydrates at the surface to form advanced oxidation products after contact with ultraviolet light.
28. The system of claim 27, wherein the surface of the at least one catalytic target structure further comprises a hydrophilic agent.
29. The system of claim 24, comprising:
a plurality of ultraviolet light sources for emitting a broad spectrum of ultraviolet light in the range of 100nm to 300nm, the ultraviolet light emitted from at least one of the plurality of ultraviolet light sources comprising ultraviolet light energy at 185nm and at 254 nm; and
a plurality of catalytic target structures, each of the plurality of catalytic target structures comprising a surface in contact with ultraviolet light from at least one of the plurality of ultraviolet light sources, the surface comprising titanium dioxide and at least one of the following metal compounds:
silver;
zinc;
copper; and
(ii) rhodium (II),
wherein the titanium dioxide is formed in an anhydrous magnesium carbonate substrate, at least one of the metal compounds is contained in a cerium oxide reinforced structure having an additional photoreaction enhancer,
and wherein the surface reacts with hydrates at the surface to form advanced oxidation products after contact with ultraviolet light.
30. The system of claim 29, wherein the surface further comprises a hydrophilic agent.
31. The system of claim 24, further comprising an ionizer for releasing positive and negative ions.
32. The system of claim 31, further comprising an ion emitter having integrated automatic purging capability.
33. The system of claim 32, wherein the ion emitter is a carbon fiber ion emitter.
34. A method for forming advanced oxidation products at a catalytic surface comprising titanium dioxide and at least one of the following metal compounds: silver, zinc, copper and rhodium, wherein the titanium dioxide is formed in an anhydrous magnesium carbonate substrate, at least one of the metal compounds is contained in a cerium oxide reinforced structure having an additional photoreaction enhancer, the method comprising:
hydrating the catalytic surface;
contacting the catalytic surface with ultraviolet light; and
forming advanced oxidation products at the catalytic surface.
35. The method of claim 34, wherein hydrating the catalytic surface comprises hydrophilically absorbing hydrates from the atmosphere surrounding the catalytic surface.
36. The method of claim 34, wherein the ultraviolet light comprises ultraviolet light energy at 185nm and at 254 nm.
37. The method of claim 34, wherein the catalytic surface comprises titanium dioxide, silver, zinc, copper, and rhodium.
38. The method of claim 34, wherein the catalytic surface comprises a hydrophilic agent, titanium dioxide, silver, zinc, copper, and rhodium.
39. The method of claim 34, further comprising using positive and negative ions to enhance the formation of advanced oxidation products.
40. The method of claim 39, further comprising automatically purging.
41. A system for forming advanced oxidation products, the system comprising:
at least one ultraviolet light source for emitting a broad spectrum of ultraviolet light in the range of 100nm to 300nm, the ultraviolet light emitted from the at least one ultraviolet light source comprising ultraviolet light energy at 185nm and at 254 nm;
at least one catalytic target structure comprising a surface in contact with ultraviolet light from the at least one ultraviolet light source, the surface of the at least one catalytic target structure comprising titanium dioxide and at least one of the following metal compounds:
silver;
zinc;
copper; and
(ii) rhodium (II),
wherein the titanium dioxide is formed in an anhydrous magnesium carbonate substrate, at least one of the metal compounds is contained in a cerium oxide reinforced structure having an additional photoreaction enhancer,
and wherein the surface of the at least one catalytic target structure reacts with hydrates at the surface after contact with ultraviolet light to form advanced oxidation products; and
a fiber optic cable mechanically coupled to each of the at least one ultraviolet light source, the fiber optic cable comprising:
a first end positioned to receive light emitted by each respective one of the ultraviolet light sources, and
a second end providing an output optical signal indicative of an operational state of the system.
42. The system for forming advanced oxidation products of claim 41, further comprising:
an ultraviolet light filtering component for substantially filtering ultraviolet light while passing visible light visible to a human, the fiber optic cable cooperating with the ultraviolet light filtering component to provide the visible light as an output optical signal from the second end of the fiber optic cable.
43. The system for forming advanced oxidation products of claim 41, further comprising:
an adjustable power supply electrically coupled to the at least one ultraviolet light source for providing an adjustable electrical power signal thereto.
44. The system for forming advanced oxidation products of claim 41, further comprising:
an ultraviolet photodetector optically coupled to the second end of the fiber optic cable for providing an output signal indicative of an operational status of at least one ultraviolet light source.
45. The system for forming advanced oxidation products of claim 44, further comprising:
an adjustable power supply electrically coupled to the at least one ultraviolet light source for providing an adjustable electrical power signal thereto; and
a controller electrically coupled with the adjustable power supply and the ultraviolet photodetector for controlling the adjustable power supply for providing an adjustable electrical power signal to the at least one ultraviolet light source in response to receiving an output data signal from the ultraviolet photodetector indicative of an operational status of the at least one ultraviolet light source.
46. The system for forming advanced oxidation products of claim 45, further comprising:
an information component coupled with the controller for sending an information/alarm signal to a user/operator/technician associated with the system in response to receiving an output data signal from the ultraviolet photodetector indicative of an operational status of the at least one ultraviolet light source.
47. The system for forming advanced oxidation products of claim 41, further comprising an ionizer for releasing positive and negative ions.
48. The system for forming advanced oxidation products of claim 47 further comprising an ion emitter having integrated auto purge capability.
49. The system for forming advanced oxidation products of claim 48 wherein the ion emitter is a carbon fiber ion emitter.
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