Method for oxygenating wastewater

Information

  • Patent Grant
  • 7294278
  • Patent Number
    7,294,278
  • Date Filed
    Friday, November 4, 2005
    19 years ago
  • Date Issued
    Tuesday, November 13, 2007
    17 years ago
Abstract
A method and apparatus creates gas-enriched fluid that is used to treat wastewater. In one embodiment, the wastewater is withdrawn from a supply of wastewater to be treated, and the wastewater is delivered in an atomized manner to a vessel pressurized with gas to form gas-enriched wastewater. The gas-enriched wastewater is then delivered to the supply of wastewater to be treated.
Description
FIELD OF THE INVENTION

The present invention relates generally to a system and method for gas-enriching water and, more particularly, to a system and method for providing large volumes of oxygen-enriched water to a reservoir, tank, pond, stream, etc. to help meet its biochemical oxygen demand.


BACKGROUND OF THE INVENTION

This section is intended to introduce the reader to various aspects of art which may be related to various aspects of the present invention which are described and/or claimed below. This discussion is believed to be helpful in providing the reader with background information to facilitate a better understanding of the various aspects of the present invention. Accordingly, it should be understood that these statements are to be read in this light, and not as admissions of prior art.


Any natural waterway has the ability to assimilate organic matter. When the loading of organic matter exceeds this assimilative capacity, the water resource is impaired for this reason. Waste, whether human or industrial, is treated for safe release into the environment. For example, wastewater from municipalities and industry is treated before discharge into waterways such as rivers. In many cases, these treatments accelerate the natural assimilation process by introducing additional oxygen to the biological process of degrading the waste.


Pollution, or contamination, of water is a serious problem throughout the world, particularly in the United States. Various sources of contamination are responsible for water pollution, including industrial and municipal entities. Industrial entities may discharge liquid or two-phase (liquid/solid) waste indirectly or directly into the environment, such as into rivers and lakes, contaminating the water supply and harming the environment, fish and wildlife. Air pollution is also a problem, particularly industrial air pollution, because airborne contaminants may be collected by rainfall and runoff into bodies of water. Industrial waste may include heavy metals, hydrocarbons, generally toxic materials, and many other known and unknown contaminants. In addition, wastewater and air pollution typically emit an undesirable odor from the contaminants, which may be a result of insufficient wastewater treatment or inefficient industrial systems (e.g., inefficient combustion, chemical reactions or processes, etc.) creating such contaminants.


Municipalities also produce considerable waste. Particularly, combined sewer overflows (CSOs), sanitary sewer overflows (SSOs), and stormwater discharges can create significant problems. Sewage carries bacteria, viruses, protozoa (parasitic organisms), helminths (intestinal worms), and bioaerosols (inhalable molds and fungi) among many other contaminants. Combined sewers are remnants of early sewage systems, which use a common pipe to collect both storm water runoff and sanitary sewage. During periods of rainfall or snowmelt, these combined sewers are designed to overflow directly into nearby streams, rivers, lakes or estuaries. SSOs are discharges of sewage from a separate sanitary sewer collection system, which may overflow prior to reaching a sewage treatment plant. Sanitary sewers may overflow for a variety of reasons, such as inadequate or deteriorating systems, broken or leaky pipes, and/or excessive rain or snowfall infiltrating leaky pipes through the ground. Finally, storm water runoff adds to the problem, as pollutants are collected en route to rivers, streams, lakes, or into combined and sanitary sewers. Storm water picks up contaminants from fertilizers, pesticides, oil and grease from automobiles, exhaust residue, air pollution fallout, bacteria from animals, decayed vegetation, and many other known and unknown contaminants.


Water contamination may be site specific, as with many industrial entities, or it may be non-site specific as with many CSOs, SSOs, and storm water runoffs. Although the discussion has been limited to industrial and municipal waste, contamination may arise from a variety of sources and accumulate in various site specific and non-site specific locations. For example, agricultural waste, pesticides and fertilizers create site specific water contamination, such as in ponds, streams, irrigation, ground water and drinking water for the animals and people.


Today, the most common waste treatment method is aerobic biological degradation, which uses microorganisms, commonly referred to as “bugs,” to biodegrade waste. In a wastewater treatment application, aerobic biological degradation typically involves an aeration/activated sludge process in which oxygen is added to one or more tanks containing the wastewater to be treated. The oxygen supports the microorganisms while they degrade the compounds in the wastewater. To enable the microorganisms to grow and degrade the waste and, ultimately, to reduce the biochemical oxygen demand (BOD), i.e., the amount of oxygen required by microorganisms during stabilization of decomposable organic matter under aerobic conditions, in the treatment system, sufficient oxygen must be available. In some systems, additional oxygen is required to also reduce nitrogen levels in the effluent.


Typically, waste treatment plants use mechanical or diffuse aerators to support the growth of microorganisms. Mechanical aerators typically employ a blade or propeller placed just beneath the surface of a pond, tank, or other reservoir to induce air into the wastewater by mixing. Such mixers generally have relatively low initial capital costs, but often require substantial amounts of energy to operate.


Alternatively, diffused aerators introduce air or oxygen into wastewater by blowing gas bubbles into the reservoir, typically near its bottom. Diffused aerators, depending upon design, may produce either coarse or fine bubbles. Coarse bubbles are produced through a diffuser with larger holes and typically range in size from 4 to 6 mm in diameter or larger. Fine bubbles, on the other hand, are produced through a diffusers with smaller holes and typically range in size from 0.5 to 2 mm in diameter. Diffused aerators typically have lower initial costs, as well as lower operating and maintenance costs, than mechanical aerators.


Mechanical and diffused aerators involve driving off volatile organic compounds (VOC's) and contributing to odor issues while transferring oxygen in a gaseous state into liquid wastewater, with oxygen transfer occurring mainly as a result of diffusion across the gas-liquid boundary. For example, in the case of diffused aerators using pure oxygen, the gas-liquid boundary is defined by the outer surfaces of the air bubbles introduced into the treatment site. Generally, fine bubble aerators are more efficient than coarse bubble and mechanical aerators due to the increased total surface area available for oxygen transfer that is associated with the fine bubbles. The performance of fine bubble aeration degrades over time if regular maintenance is not used.


However, more efficient apparatus and methods for oxygenating wastewater still are needed. Municipal wastewater needs typically grow as the municipality grows in population. To meet increasing needs, municipalities either expand existing wastewater treatment facilities or build additional wastewater treatment facilities. Either option requires additional land and new equipment. Thus, much expense may be saved by enhancing the operating efficiency of existing facilities in response to increased demand for wastewater treatment.


A municipal wastewater treatment process, for example, typically involves a primary treatment process, which generally includes an initial screening and clarification, followed by a biological treatment process, sometimes referred to as a secondary treatment process. The wastewater entering the activated sludge process may have about sixty percent of suspended solids, thirty percent of BOD, and about fifty percent of pathogens removed in the primary treatment (although in some processes primary clarification may be omitted so that the solids otherwise removed are available for food for the microorganisms working in the secondary process).


The activated sludge process typically consists of one or more aeration tanks or basins in which oxygen is added to fuel the microorganisms degrading the organic compounds. After leaving the aeration tank(s) the water enters a secondary clarifier in which the activated sludge/microorganisms settle out. After passing through this activated sludge process the water typically has about 90% of the suspended solids and 80-90% of the BOD removed. The water is ready for either more advanced secondary or tertiary treatments, or for return to a natural waterway. The choice typically depends upon the effluent levels and local regulations.


Alternately, wastewater treatment may occur in a sequencing batch reactor (SBR). SBR treatment generally is the same as an activated sludge system, except that the process is performed in only one tank, whereas activated sludge systems may use several tanks. SBRs may be used as an alternative to an activated sludge process, in regular secondary treatment, or for more advanced treatment processes, e.g., nitrification/denitrification and phosphorus removal. SBRs may process numerous batches per day. Typically, for industrial applications SBRs process one to three batches per day, whereas for municipal applications SBRs may process four to eight batches per day.


The operation of an SBR generally includes five separate phases: fill, react, settle, decant, and idle, although there may be alternatives to these SBR phases depending upon the circumstances involved in a particular application. In the fill phase, wastewater enters the reactor tank through a port near the bottom of the basin, after which the inlet valve is closed. Aeration and mixing may begin during the fill. In the react phase, the inlet is closed and aeration and mixing continues or begins. In the settle phase, the remaining solids settle to the bottom of the basin. In the decant phase, fluid is removed from the surface of the basin by a decanter. During this time settled sludge also may be removed. In the idle phase, the reactor awaits a new batch of wastewater, typically with a portion of the biomass remaining in the basin to provide food for the microorganisms in the next batch.


The owners and operators of wastewater treatment plants often search for ways to lower the cost of remaining in compliance with local, state, and/or federal laws regulating such plants. One way of lower operating costs has been to pursue energy conservation measures to achieve lower operating and maintenance costs. One particular target has been the substantial electricity and other energy costs associated with the operation of conventional systems for aerating wastewater. Aeration can account for more than half of municipal wastewater treatment energy consumption. However, despite past focus on improving oxygen delivery systems to deliver higher levels of oxygen into wastewater more efficiently, there remains a need for further improvement, i.e., an apparatus and method for delivering large quantities of oxygen in conjunction with wastewater treatment applications. Furthermore, a flexible waste treatment apparatus and method is needed to adequately address non-site specific water pollution, for example, in stream water pollution resulting from CSOs, SSOs and storm water runoff, and special and/or smaller applications such wastewater and odor control on farms.


SUMMARY OF THE INVENTION

The present invention may address one or more of the problems set forth above. Certain possible aspects of the present invention are set forth below as examples. It should be understood that these aspects are presented merely to provide the reader with a brief summary of certain forms the invention might take and that these aspects are not intended to limit the scope of the invention. Indeed, the invention may encompass a variety of aspects that may not be set forth below.


A system is provided for transferring gas into fluids. In one embodiment, the system is an assembly for delivering oxygen into wastewater. The system includes an oxygenation assembly including a pressurizable chamber that receives water from a fluid supply assembly and oxygen gas from an oxygen gas supply assembly. Advantageously, the oxygen gas supplied pressurizes and maintains the chamber at a pressure greater than atmospheric pressure (e.g., 300 p.s.i.). The water advantageously enters the chamber through an atomizer nozzle that forms water droplets within the chamber. As the water droplets fall within the chamber, oxygen diffuses into the droplets, which collect as a pool of oxygen-enriched water at the bottom of the chamber. The oxygen-enriched water is removed from the chamber and delivered via a hose to a treatment site.


It should be understood that the water to be oxygen-enriched may be relatively clean water from a water supply, such as a tank, pond, lake, stream, or river. Once this relatively clean water is oxygen-enriched, it may be added to the wastewater to raise the oxygen level of the wastewater. Alternatively, the water to be oxygen-enriched may be wastewater skimmed from the treatment tank. The skimmed wastewater is filtered to prevent the system from clogging, and the filtered wastewater is then oxygen-enriched and returned to the wastewater tank to raise the oxygen level of the wastewater in the tank.


Advantageously, the distal end of the hose includes or is coupled to a delivery nozzle including one or more capillaries through which the oxygen-enriched water effluent passes. The capillaries may be dimensioned to an appropriate length and diameter for a desired flow rate, oxygen concentration, and other flow characteristics such as substantially laminar and bubble free flow. The capillaries are advantageously made of silica, and may be dimensioned to a length of about 6 cm and an internal diameter of about 150 to 450 microns. Alternatively, the capillaries may be constructed from a variety of metals, metal alloys, glasses, plastics/polymers, ceramics or other suitable materials. For an oxygen-enriched water flow rate of about 1.5 gal/min, at about 300 p.s.i., a delivery nozzle including approximately 450 such capillaries is particularly advantageous. The capillaries tend to stabilize the gas-enriched water during its delivery into host liquids at ambient pressure. As a result, nucleation and bubble formation in the effluent, during ejection from the capillary and mixing with the host liquid, is minimal or absent despite potentially high gas partial pressures of the oxygen dissolved in the effluent. An extremely high oxygen transfer efficiency, approaching or even equaling 100 percent, is thereby achievable with this approach for oxygenating host liquids such as wastewater.


Alternately, the oxygen-enriched water is delivered to a treatment site via a hose coupled to a plate-based delivery nozzle system. The plate-based nozzle includes one or more plates having a plurality of channels formed therein. The cross-sectional profile of the channels may be a variety of shapes, e.g., circular, square, rectangular, oval, triangular, etc. Advantageously, the channels in each plate extend along a portion of the top surface of the plate from a hole in the plate (which advantageously extends between the top and bottom surfaces of the plate) to the plate's edge. The plates are disposed on top of one another such that the bottom surface of one plate is mated to the top surface of an adjacent plate to create fluid pathways between adjacent plates. Further, by placing a bottom plate without a hole beneath a stack of plates, and by placing a top plate including a port adapted to couple to the hose on top of the stack, a plenum is formed within the stack to receive the oxygen-enriched water from the hose and to provide oxygen-enriched water to each of the fluid pathways for delivery to the treatment site.


Depending upon the circumstances involved in a particular application, a number of different geometries may be used for the plate-based nozzle system. The plates may be of any suitable size or shape, depending upon the application involved. The channels may extend in each plate to any of the sides of the plate, so that oxygen-enriched water may be delivered in any direction. Further, adjacent surfaces of two plates may have channels formed therein, so as to create a desired fluid pathway geometry when the plate surfaces are brought together, e.g., by alignment of the channels on two separate plates.


An alternate embodiment of the plate-based delivery nozzle system may employ one or more conical plates to create an annular array of fluid pathways. The conical plates have a plurality of channels, which extend linearly along an inner or outer surface between a small and broad end of the conical plates. The conical plates stack in series such that the outer surface of one conical plate is disposed within the inner surface of another conical plate, thereby creating an annular array of fluid pathways between adjacent conical plates. The conical plates are then truncated at one end to provide a common entry position for the oxygen-enriched water and are configured such that the opposite end forms a desired exit surface (i.e., conical, concave, flat, etc.). The conical plate design may advantageously simplify assembly, as the oxygen-enriched water flow forces the conical plates together during use, and may simplify cleaning, as reversed water flow may be used to separate and clean the conical plates.


By placing one or more delivery nozzles at a treatment site, oxygen levels at the site advantageously may be maintained or increased by delivering oxygen-enriched water to the site. For example, in a wastewater treatment reactor, oxygen-enriched water may be added to the reactor contents to help support biological degradation activity, reduce biochemical oxygen demand, etc. Advantageously, the water used to supply the oxygen-enriched fluid supply system is filtered to minimize the risk of the delivery nozzle becoming clogged by particulate matter. The water used to supply the system may come from any source, e.g., a municipal water source; a river, lake, or other reservoir; the treated water effluent of a wastewater treatment operation; the supply of wastewater to be treated, etc.


Because much of the oxygen provided to a treatment site is in the form of oxygen-enriched water having high levels of dissolved oxygen, oxygenation of the site occurs rapidly as the oxygen-enriched water mixes with the wastewater. Advantageously, delivery of the oxygen-enriched water occurs with minimal bubble formation, so oxygenation efficiencies are achieved which surpass the efficiencies obtainable with commercially available aerators. Thus, the system provided advantageously may be used either to replace or to supplement conventional aeration equipment.





BRIEF DESCRIPTION OF THE DRAWINGS

Further objects and advantages of the present invention may become apparent upon reading the following detailed description and upon referring to the accompanying drawings in which:



FIG. 1 is a schematic diagram illustrating an exemplary embodiment of a system for oxygenating wastewater including an oxygen-enriched fluid supply system in accordance with the present invention.



FIG. 2 is a schematic diagram illustrating an exemplary embodiment of an oxygen-enriched fluid supply system in accordance with the present invention.



FIG. 3 is a view of an exemplary embodiment of an oxygen-enriched fluid supply system including an exemplary fluid supply cart and an exemplary oxygenation cart in accordance with the present invention.



FIG.4 is a cross-sectional view of an exemplary oxygenation assembly in accordance with the present invention.



FIG. 5 is a cross-sectional view of an alternate exemplary oxygenation assembly in accordance with the present invention.



FIG. 6A is an end view of one embodiment of a gas-enriched fluid delivery nozzle.



FIG. 6B is a cross-sectional side view of the nozzle of FIG. 6A.



FIG. 7 is an end view of an alternative embodiment of a gas-enriched fluid delivery nozzle, along with an enlarged view of a portion of the nozzle.



FIGS. 8A-E illustrate another alternative embodiment of a gas-enriched fluid delivery nozzle, particularly illustrating a plate-based nozzle.



FIGS. 9A-F illustrate exemplary channel geometries that may be used in conjunction with a plate-based nozzle, such as the nozzle shown in FIGS. 8A-E.



FIG. 10 illustrates an exemplary clamping assembly that may be used in conjunction with a plate-based nozzle, such as the nozzle shown in FIGS. 8A-E.



FIG. 11 illustrates a wastewater treatment plant utilizing a system for oxygenating wastewater including an oxygen-enriched fluid supply system in accordance with the present invention.





DETAILED DESCRIPTION OF SPECIFIC EMBODIMENTS

The description below illustrates certain specific embodiments or forms that depict various aspects of the present invention. For the sake of clarity, not all features of an actual implementation are described in this specification. It should be appreciated that in connection with developing any actual embodiment of the present invention many application-specific decisions must be made to achieve specific goals, which may vary from one application to another. Further, it should be appreciated that any such development effort might be complex and time-consuming, but would still be routine for those of ordinary skill in the art having the benefit of this disclosure.


For the sake of clarity and convenience, the various embodiments are described herein in the context of applications generally involving municipal wastewater treatment, including treatment of CSOs, SSOs, and storm water discharges. However, the present invention may also be useful in other applications, such as industrial wastewater treatment, e.g., in the petroleum, food, pulp and paper, and steel industries; lake and stream restoration and/or wastewater treatment; chemical wastewater treatment; landfill wastewater treatment; ground water treatment; drinking water disinfection with ozone; agricultural or aquacultural water treatment; odor control (e.g., on farms); etc. Also, although the present system may be used to raise gas levels, such as oxygen for example, in water or other fluids, for the sake of clarity and convenience reference is made herein only to wastewater applications.


It should be understood that the gas supplied by the gas supply assembly described below may include oxygen, ozone, carbon monoxide, carbon dioxide, hydrogen, nitrogen, air, chorine gas, and/or other treatment gases, while the gas-enriching assembly described below advantageously includes a gas-absorption assembly capable of raising the dissolved gas content of the fluid provided by the fluid supply assembly described below. However, again for the sake of clarity and conciseness, the use of oxygen gas will be primarily discussed herein by way of example.


Turning now to the drawings, a wastewater treatment system is provided in which, as shown in FIG. 1, wastewater influent is delivered to a reactor 10 for primary treatment. Advantageously, the wastewater includes microorganisms for carrying out an aerobic biological degradation process. To support microorganism activity, the wastewater is oxygenated. To provide such oxygenation, a conventional aeration system 20, e.g., a mixer or diffuser, and an oxygen-enriched fluid supply system 30 are illustrated, although it should be understood that the fluid supply system 30 may be used alone or in conjunction with the conventional aeration system 20. Advantageously, the system 30 or the systems 20 and 30 are operated to meet the BOD for the reactor 10. After an initial screening and clarification, wastewater from the reactor 10 is typically transferred to a secondary clarifier 40 for further treatment. A second oxygen-enriched fluid supply system 50 may be used, again either alone or in conjunction with a conventional aeration system (not shown in FIG. 1), to raise or maintain oxygen levels in the clarifier 40 to support microorganism activity. After sufficient processing to achieve predetermined levels of suspended solids and BOD, supernatant treated water is removed as an effluent and all or a portion of the settled waste sludge is removed for disposal, with any remaining sludge returned to the reactor 10 to join a new batch of influent for treatment.


As shown in FIG. 2, one exemplary embodiment of an oxygen-enriched fluid supply system 30 includes a gas-enriching assembly, such as an oxygenation assembly 60, operatively coupled to both a gas supply assembly, such as an oxygen gas supply assembly 70, and a fluid supply assembly 80. The oxygenation assembly 60 advantageously includes an oxygen absorption assembly capable of raising the dissolved oxygen content of the fluid provided by the supply assembly 80. The oxygen-enriched fluid exiting the oxygenation assembly 60 advantageously is provided to an oxygen-enriched fluid delivery assembly 90 for transfer to a predetermined treatment site.


Dissolved oxygen levels of the fluid may be described in various ways. For example, dissolved oxygen levels may be described in terms of the concentration of oxygen that would be achieved in a saturated solution at a given partial pressure of oxygen (pO2). Alternatively, dissolved oxygen levels may be described in terms of milligrams of oxygen per liter of fluid or in terms of parts per million of oxygen in the fluid.


As shown in FIG. 3, one currently assembled embodiment of an oxygen-enriched fluid supply assembly 30 includes a fluid supply cart 100 operatively coupled to an oxygenation cart 200. The carts 100 and 200 support various respective components of the system 30 and demonstrate that the system 30 may be small enough to be mobile. Of course, the actual size of the system 30 and the mobility or lack thereof of the system 30 will depend primarily upon the requirements of a given implementation. For example, if the system 30 were to be used as the sole means for aerating a reactor 10 in a municipal wastewater facility, it would likely be embodied as a fixture at the site. However, if the system 30 were to be used for aerating ponds or as a supplemental aerator in an industrial or municipal wastewater facility, it may be advantageous to mount the various components of the system 30 on a moveable cart or plat, or even on a trailer or vehicle (not shown).


Water is provided to the fluid supply cart 100 at via line 102 from a source, e.g., the reactor tank 10, a holding tank, a municipal water supply line, etc., or by a pump withdrawing the water from a tank, pond, stream, or other source. Advantageously, for an application involving wastewater treatment, the water is input at a rate of between about 5 and about 200 gallons per minute, although the input rate may be higher or lower depending upon the application. More specifically, a rate of about 60 gallons per minute may prove to be particularly advantageous for many applications. The provided water advantageously is filtered to remove solid particulate. To provide this function, one or more filters, such as the filters 104 and 106, are coupled to the line 102. It should be understood that multiple filters may be coupled in series or in parallel depending upon the circumstances involved in a particular application. As discussed below, a series of filters may be used to remove particulate matter from the incoming water effectively. It may also be advantageous to couple filters or sets of filters in parallel so that one or more filters can be serviced without stopping the treatment process.


In a wastewater treatment application, at least one filter (e.g., a 150 to 450 micron filter) may prove to be particularly advantageous, although it should be understood that the type and number of filters used may depend largely upon the source of the water to be oxygenated. For instance, if relatively clean water from a holding tank is to be oxygenated, a single filter, such as a 150 micron filter, may be sufficient to remove particulate matter. However, if wastewater is skimmed off of the reactor 10 and introduced into the system 30, additional filters, such as a coarse filter (e.g., 450 micron) and a medium filter (e.g., 300), may be used to remove large particulate matter before the partially filtered water is introduced to a relatively fine filter, such as a 150 micron filter. Examples of commercially available filters include sand filters, cartridge filters and bag filters, which may be self-flushing or may contain disposable elements such as cotton, plastic, metal or fiber filter elements. Also, the filter size is typically selected to be the same as or smaller than the capillaries used to deliver the oxygenated fluid.


As shown in FIG. 3, the filtered water advantageously is provided to a holding tank 108, e.g., a 300-gallon tank, via a line 110 that is coupled to the fluid exit ports of the filters 104 and 106. Advantageously, a valve 111, such as an electronic valve, is operatively coupled to the line 110 supplying the tank 108 to help control flow into the tank 108 based upon the level of water in the tank 108. Such control might occur, for example, in response to signals generated by one or more level sensors positioned for controlling the level of water in the tank 108, or by a load cell operatively linked to the tank 108. The tank 108 also may include high and low water sensors for safety shut-off.


Fluid exits the tank 108 through a primary line 112 (e.g., by gravity feed) to a pump 114 run by a motor 116. The pump 114 provides the fluid to the oxygenation cart 200 via a line 118. The fluid may be filtered before and after the pump 114 to remove additional particulate matter. As shown in FIG. 3, the line 118 includes a 150 micron filter 202 disposed on the oxygenation cart 200. In addition, the pump 114 may be operatively coupled to an assembly 115, such as an accumulator, for dampening the pulsatility created by the pump 114 so that the fluid is provided to the oxygenation cart 200 at a steady, continuous rate during pump operation.


The pump 114 can run continuously or intermittently, and can provide variable or constant flows, depending upon the circumstances involved in a particular application. One example of a particularly advantageous pump is the model #60AG6020 pump available commercially from CAT Pumps, Minneapolis, Minn. To regulate the amount of flow provided to the oxygenation cart 200 for oxygenation, the line 118 via which fluid is provided to the oxygenation cart 200 may include a modulating valve 119, such as an electronic valve, operable as needed to divert a predetermined portion of the flow via a bypass line 204 back to the tank 108. The oxygenation cart feed line 118 advantageously includes a check valve 121 to prevent unwanted flow of gas or liquid from the oxygenation cart back toward the pump 114 and tank 108.


The system also may include a flush line 230 between the tank and the delivery assembly which bypasses the oxygenation assembly. The flush line 230 allows water to pass to prevent dirty water from back flowing into the system when the oxygenation assembly is in stand-by mode. As shown in FIG. 3, the flush line 230 advantageously also may provide a fluid pathway between the lines 110 and 224.


The oxygenation cart 200 advantageously includes a pressurizable vessel 210 that has an interior space 212 in which water from the pump 114 and gas from a gas supply assembly (not shown) are provided. The water enters the vessel 210 from the feed line 118 via a cantilever-like “stinger” 214 (see FIG. 4) extending from the top of the vessel 210 into the interior space 212. The stinger 214 advantageously comprises a 1.5 inch pipe 215 about 3 feet in length having an inner lumen (not shown) in fluid communication with the feed line 118. The stinger 214 includes one or more nozzles 216 that form fluid ports through which fluid may exit the stinger's inner lumen and enter the interior space 212. In one embodiment, each nozzle takes the general form of a pig tail which winds to form a generally conical profile.


The stinger 214 includes one or more nozzle arrays 218 including a plurality of nozzles 216 arranged about the longitudinal axis of the stinger 214. In the disclosed embodiment, each nozzle array 218 includes six nozzles 216 equally circumferentially spaced about the longitudinal axis of the stinger 214. The stinger 214 may include a plurality of nozzle arrays 218 spaced along the longitudinal axis of the stinger 214. As shown in the embodiment illustrated in FIG. 4, the stinger 214 includes six arrays of six nozzles spaced about six inches apart along the stinger 214. Advantageously, the nozzles in the arrays may be circumferentially offset from each other to minimize any overlap in the fluid exit area of each nozzle. This minimizes interference between water droplets from adjacent nozzles and, thus, facilitates the production of smaller droplets to optimize gas transfer to the liquid. Alternatively, an umbrella (not shown) may be placed over one or more nozzle arrays to minimize interference between water droplets.


Each nozzle 216 advantageously comprises an atomizer nozzle. Any commercially available atomizer nozzle may be used depending on the circumstances involved in a particular application. One particularly advantageous nozzle is the Model TF6NN 3/16 stainless steel (0.25 inch npt) fog nozzle available from BETE Fog Nozzle, Greenfield, Mass. During operation, water exiting the nozzles 216 forms a spray of small droplets which contact the oxygen gas in the chamber. Oxygen dissolves in the droplets, which fall and collect in a pool at the bottom of the oxygenation assembly chamber. The pool advantageously is about two feet deep in a twelve-inch diameter chamber that is about six feet tall. Furthermore, the number and size of the nozzles are typically selected to provide a desired throughput. Indeed, should throughput parameters change, one or more valves (not shown) may be placed in the pipe 215 to selectively activate or deactivate one or more of the nozzle arrays.


The stinger 214 advantageously is removably insertable within the interior space 212. The stinger 214 may be secured in place for operation by fastening the inlet end to the top of the oxygenation assembly, e.g., with bolts or other fasteners. Removal may be advantageous to allow access to the interior of the oxygenation assembly 210 and to the stinger 214, e.g., to clean the nozzles, to replace nozzles or other parts, etc.


Oxygen is provided to the oxygenation assembly by a regulated source of oxygen. Advantageously, the oxygen gas is provided to the oxygenation assembly 210 at about 300 p.s.i. via a line which includes a valve regulating the flow through the line and a check valve that prevents unwanted back flows. The pressure and/or flow through the line may fluctuate with changes in the water level within the oxygenation assembly 210.


Water is provided to the oxygenation assembly 210 at a pressure greater than the pressure in the tank interior space 212—about 300 p.s.i. in this example. A steady state water supply pressure of about 340 p.s.i. may prove to be particularly advantageous for applications involving wastewater treatment, although pressure fluctuations commonly occur during operation of the system. Advantageously, the oxygenation assembly 210 includes one or more pressure gauges to allow monitoring and control of the pressures in the system. The oxygenation assembly 210 and other parts of the system further advantageously include one or more pressure relief valves to guard against unwanted pressure build-ups within the system.


In this embodiment, fluid exits the oxygenation assembly chamber through a dip tube 222 having an inlet end 224 positioned above the bottom of the chamber. By removing fluid from near the bottom of the chamber (as opposed to at the top), gas blow-by is avoided and no bulk gas exits the chamber. The dip tube 222 is connected to an output line 224 having a distal end coupled to a delivery assembly, so as to create a continuous fluid flow path between the pool in the chamber and the delivery assembly inlet. The output line 224 may include one or more valves, check valves, and/or filters. For example, as shown in FIG. 3, the line 224 includes a 150 micron filter 226.


Advantageously, the oxygenation assembly 210 also includes one or more windows or sight glasses 220 which allow an operator to view the interior of the oxygenation assembly 210 during operation. Visual monitoring may be performed, for example, to check the operation of the nozzles (e.g., to monitor fluid droplet sizes, check for plugging resulting in flow disruption, etc.), to check fluid levels, etc.


In this example, the fluid collecting at the bottom of the chamber has a dissolved gas content of about 880 ppm. This dissolved oxygen content represents an increase in oxygen content of about one hundred times as compared to the fluid entering the chamber before oxygenation. The dissolved gas concentration, along with the operating efficiency, costs, and flow characteristics of the system, may be widely varied according to the operating parameters (e.g., fluid and gas pressures) of the disclosed embodiments. For example, the apparatus could produce a dissolved gas content ranging from approximately 40 ppm to 8000 ppm for system pressures ranging between about 14.7 and 3000 p.s.i., depending on the given operating parameters and system limitations. It should also be pointed out, that lowering pressures within the system lowers the amount of dissolved gas content that is achievable, but the lower pressures also lower the cost of the system. For example, if the system pressures were lowered by about 200 p.s.i. from the 300 p.s.i. range to the 100 p.s.i. range, the dissolved gas content of the fluid would be about 275 ppm. In many applications, this oxygen-enriched fluid will be more than adequate to aerate the wastewater, while providing lower equipment and operating costs.


As one alternative configuration, the oxygenation assembly 60 may include a plurality of nozzles 250 disposed circumferentially about the wall of a tank 252, as illustrated in FIG. 5. Advantageously, the flow of fluid entering the tank 252, e.g., from a fluid inlet manifold 254, via the nozzles 250 is controlled by a valve 256 adjusted in response to signals generated by sensors (not shown) for detecting the level of water in the tank 252, or by a load cell (not shown) disposed beneath the tank 252. Oxygen from a regulated pressure source (not shown) enters the tank 252 at the top, and oxygen-enriched fluid is withdrawn via a fluid exit port 258 at or proximate the tank bottom. In an application including a tank about 5 feet high and 2 feet in diameter (a tank size of about 100 gallons), for fluid flow rates of about 15 gallons per minute, a system including four nozzles 250 capable of handling two to four gallons per minute and generating a droplet cone defined by an included angle α of about 90 degrees may prove to be particularly advantageous. For higher fluid flow rates, e.g., 60 gallons per minute, a system including eight nozzles for handling six to eight gallons per minute may be advantageous.


One embodiment of the oxygen-enriched fluid delivery assembly 90 may include one or more elongated hoses 301 (FIG. 3) having a proximal end including a fluid inlet coupled to the output of the tank of the oxygenation assembly 60 and a distal end including one or more fluid exit nozzles 303. The hose length may vary depending upon the circumstances involved in a particular application. Advantageously, the fluid exit nozzle 303 comprises a plurality of capillaries, channels, or slits forming continuous fluid pathways that are sized to maintain the oxygen dissolved in the fluid upon exit.


In one embodiment, as shown in FIG. 6A, the fluid exit nozzle 303 comprises a collar assembly 300 comprising a main body portion 302 adapted with a plurality of fluid exit pathways 308. The portion 302 may be adapted with a quick couple/disconnect assembly for coupling to the distal end of the oxygen-enriched fluid delivery hose 301. Alternately, as shown in FIG. 6B, the main body portion 302 may include a female threaded portion 304 (advantageously having about 8 threads per inch) for receiving the distal end of the hose 301. An o-ring 306 is used to seal the hose coupling to prevent fluid from the hose from bypassing the exitways 308. Advantageously, the nozzle may be configured to have an outer diameter of about 3 inches; a length of about 2 inches; and up to 500 or more fluid exitways, each about 1.5 inches long and 0.005 inches in diameter. It should be noted that the fluid channels in the fluid exit nozzle 303 advantageously exhibit a cross-sectional area and a length that is chosen to substantially prevent bubble formation and to provide laminar flow of the gas-enriched fluid upon exit from the nozzle 303.


Alternately, as shown in FIG. 7, the fluid exit nozzle 303 advantageously comprises a plurality of small capillaries 310, which may be grouped into tubes 312. For example, each of the capillaries 310 may have an inner diameter of about 150 to 450 microns, and may be disposed with the tubes 312 in groups of about sixty capillaries 310. Each tube 312 is formed by extruding silica over the top of the sixty capillaries 310 as they are brought together, so as to create a capillary bundle within a tube. The tubes 312 advantageously are fixedly attached to each other (e.g., with an epoxy) at their outer surfaces to create a tube bundle. The tube bundle advantageously is about five inches long and about an inch in diameter.


To clean the capillary inlets, the distal end of the hose may include a valve (not shown) that can be opened and closed as desired to allow water to flow rapidly across the capillary inlets to the treatment site. In another embodiment, the capillaries may be flushed by creating a venturi effect that creates backflow in a capillary being cleaned. Alternately, each tube bundle can be replaced and cleaned separately.


In one alternate embodiment illustrated in FIGS. 8A-8E, the fluid exit nozzle 303 may comprise a plate assembly 320 including a stack of plates 322. The plates 322 have a plurality of channels 324 along at least a portion of one side between an edge and a hole in the plates 322. A variety of channel configurations may be suitable, such as those illustrated in FIGS. 9A-F. When a plurality of like plates 322 are joined on top of each other with edges aligned, a block 326 is formed having a hole 328 therethrough. A plurality of channels 324 extend through the block 326 to the hole 328. When a bottom plate 330 without a hole and a top plate 332 including a port 334 are placed on the block 326, a plenum is created.


As illustrated in FIG. 10, the plates 322 may be placed in an assembly 350 operable to separate the plates 322 as desired to permit cleaning. The surfaces of the plates 322 exposed to fluid during operation advantageously are smooth (e.g., as a result of polishing) and are cleaned with alcohol prior to use, so as to minimize the number of sites at which bubbles may nucleate and grow.


Rather than using flat plates, an alternate embodiment may employ one or more conical plates to create an annular array of fluid pathways. The conical plates have small and broad ends, inner and outer surfaces between the ends, and a plurality of channels extending between the ends on at least one of the surfaces. The channels may extend linearly or curvilinearly between the small and broad ends, and they may assume a variety of cross-sections and spacings along the surfaces. The conical plates stack in series such that the outer surface of one conical plate is disposed within the inner surface of another conical plate, thereby creating an annular array of fluid pathways between adjacent conical plates as the channels are enclosed by the adjacent inner or outer surfaces. The conical plates are then truncated at the small ends to provide a common entry position for the fluid pathways. Oxygen-enriched water enters at the common entry position, flows through the fluid pathways and disperses at the broad ends. The conical plates may be designed such that the broad ends form a particular exit surface, for example, flat, concave, or conical, which may improve flow characteristics, provide a specific spray pattern, or alter other characteristics. Alternatively, the conical plates may be configured such that the oxygen-enriched water enters at the broad end, truncated and aligned to form the common entry position, and exits at the small end.


The conical plate design is advantageous for simplifying assembly, since the conical plates are easily aligned, stacked and secured without a separate mounting apparatus. Properly configured, the oxygen-enriched water flow advantageously forces the individual conical plates together during use, thereby maintaining close contact of the surfaces. The conical plate design is also advantageous for cleaning, which may be achieved by backflushing the conical plate assembly. By reversing the flow through the conical plate assembly, the individual conical plates are forced to separate, and debris is washed away.


The system for oxygenating wastewater including an oxygen-enriched fluid supply system may be used in a wastewater treatment system, such as a municipal wastewater treatment plant 400 illustrated in FIG. 11. Specifically, the system may be utilized in one or more of the aeration tanks 402 or clarifier tanks 404. It should be noted that the nozzle(s) 303 of the system may be placed in the tanks 402 and/or 404 to provide oxygen-enriched fluid to the wastewater contained therein. In this situation, it may be desirable to include one or more mixers (not shown) in the tanks 402 and/or 404 in the vicinity of the nozzle(s) 303 to facilitate oxygenation of the wastewater therein. Alternatively, the nozzle(s) 303 may be placed in a secondary tank 406 located separate from the tanks 402 and 404. In this situation, the oxygenated water flows into the secondary tank 406, which then delivers the oxygenated water into the associated tank 402 or 404 via an appropriate delivery system, such as a gravity fed line(s) or a pump and line(s) combination. As mentioned above, it may be desirable to include one or more mixers (not shown) in the tanks 402 and/or 404 in the vicinity of the line(s) to facilitate oxygenation of the wastewater therein. By keeping the nozzle(s) 303 out of the wastewater in the tanks 402 and 404, the nozzles will remain much cleaner and, thus, generally operate more efficiently.


Although numerous embodiments have been disclosed for treating contaminated water, many modifications are contemplated to address specific wastewater treatment applications requiring gas-enrichment. Wherever aeration of water is required to treat wastewater, the disclosed embodiments, or modified versions thereof, scaled to produce a desired flow rate of oxygen or air-enriched water, may advantageously increase the oxygen content of the wastewater. Compared with conventional aeration techniques, which use diffusion between the liquid/gas interface (i.e., bubbles), the disclosed embodiments are advantageously efficient in transferring gas to gas-depleted host liquids, while providing relatively good control of the level of dissolved gas in the host liquid. Additionally, the disclosed embodiments may advantageously reduce odors from the wastewater and from the gases applied to the wastewater (e.g., by more effective treatment and/or by reducing the amount of gas escaping, or bubbling out, into the environment).


Recognizing these advantages, among many others, various embodiments may be used for water treatment in agricultural and aquacultural sites. For example, animal farms, particularly pig farms, typically generate considerable waste in a concentrated area, making waste management, odor control and water contamination a problem. Where crops are grown and cultivated, fertilizers and pesticides may contaminate the water, for example, by running off the crops and land with rainfall. These water quality problems are compounded by odor concerns, standard aeration techniques contribute to the problem. Similarly, marine tanks, fish farms, and hatcheries typically concentrate marine life in a relatively small tank, pool or body of water, wherein water quality and oxygenation may become a problem. In specialized applications such as these, where conventional treatment techniques may be insufficient, too costly, or generally undesirable, the disclosed embodiments advantageously provide a flexible and potentially economical solution to water treatment. To reduce costs, atmospheric air or compressed air may be used rather than pure oxygen. For example, it may be more economical to use an air compressor where the apparatus is used for aerating large bodies of water, such as rivers, ponds and lakes. The disclosed embodiments may also be designed as, or retrofitted to, a mobile deployment system, which may be moved from one treatment site to another. The mobile deployment system may be removably or fixably mounted to a truck, to a trailer, to a boat or other watercraft, to an aircraft such as a helicopter, to carts as disclosed above, or any reasonably mobile unit. A mobile system such as this would be flexible and quite advantageous for non-site specific and/or emergency applications.


A variety of applications may require alternative gases, other than air or oxygen, to address specific contaminants, purify the water or wastewater, or generally, to attain desired properties of the water or wastewater. For example, anaerobic bacteria are used in some bioreactors to synthesize organic compounds, with dissolved carbon monoxide as a carbon source. Unlike carbon dioxide, both carbon monoxide and oxygen are only sparingly soluble in water. As a result, conventional techniques, such as bubbling or mixing, may fail to provide sufficient carbon monoxide to keep pace with the metabolic capacity of the anaerobic bacteria. In contrast, a modified system applying the presently disclosed embodiments could enrich the water or wastewater with carbon monoxide at a relatively high transfer efficiency, advantageously approaching 100 percent.


The disclosed embodiments also reduce gas loss, which may be costly and undesirable in many applications. Conventional techniques often involve bubbling a gas through a liquid, providing minimal gas-to-liquid transfer and considerable gas loss as the gas bubbles exit the liquid. The presently disclosed techniques provide efficient gas-to-liquid transfer, and do so in isolation from the host liquid, i.e., a host water environment such as a pond, reservoir, etc., and drive off VOC's and odors. Provided that the solubility limit of the gas in the host water is not exceeded, bubbles are essentially eliminated, and only gas-enriched water is delivered to the host water. Furthermore, the transfer rate is primarily dependent on the flow rate through the disclosed embodiments, rather than the relatively slow diffusion rate limiting conventional techniques. The substantial reduction of bubbles and improved gas to liquid transfer is also advantageous to controlling undesirable odors, which are partially caused by the wastewater and partially due to gas odors (e.g., in conventional techniques, where alternative gases are bubbled through the wastewater) from incomplete gas to liquid transfer.


Accordingly, alternative embodiments may effectively employ gases such as ozone, carbon monoxide, chlorine gas, inert gas, or other useful gases. For example, ozone may be used to disinfect or sterilize a liquid such as water, by oxidizing contaminants out of the liquid. Contaminants such as lead and cyanide, among others, may be effectively ozonated out of a liquid and into an insoluble compound, while any excess from the ozonation process generally reduces to ordinary oxygen. Ozone may also be used to reduce contamination and waste involved with materials production and processing, such as anodizing aluminum, cross-linking of synthetic polymers and natural fibers such as collagen, and bleaching processes found in paper production. In the anodizing process, ozone saturated solvents could be used instead of acids, thereby reducing the toxicity of waste materials. For further example, hydrogen gas-enriched water may be used to enhance the degradation of chlorinated solvents in groundwater. Alternatively, water enriched with alternative gases, such as ozone, chorine or gases “toxic” to certain organisms, may be employed in open bodies of water to treat specific problems, such as the eradication of zebra mollusks that clog water vents in the Great Lakes.


Because the embodiments permit delivery of a liquid highly enriched with a gas to be delivered to a host environment without immediate nucleation in the effluent from the nozzles, the gas concentration of the host environment, whether an empty reservoir or a host liquid, can be raised to hyperbaric levels. Numerous applications that take advantage of this effect are now possible, as a result. Several examples follow.


In wastewater treatment, increasing the air or oxygen concentration of the host liquid to hyperbaric gas concentrations results in heterogeneous nucleation in the host liquid. The nucleation will typically take place on suspended particles, including ones of microscopic size. The growth of bubbles on these particles then results in flotation of the particles, as they are carried upward by the buoyancy of the bubbles, to the upper layers or surface of the host liquid. Skimming the surface of the host liquid can then be used to remove the particulate. This process is more efficient than simply bubbling the host liquid from, for example, an aeration diffuser plate at the bottom of the host liquid. The preformed bubbles will not attach to the small particles with an efficiency comparable to the advantageous efficiency of the heterogeneous nucleation process provided by the present embodiments.


Use of the embodiments to increase the oxygen concentration of the host liquid to hyperbaric levels is advantageous in numerous oxidation processes. For example, removal of heavy metals and sulfides in polluted water, which can be initiated with addition of a peroxide, can be enhanced by high oxygen concentrations in the water as provided by the embodiments, thereby reducing the need for the peroxide. This is an advantage, since leftover peroxide is toxic to biologic organisms.


In many bioreactor applications, wherein yeast, fuigi, or bacteria require oxygen to produce a desired product or result, the ability to provide high levels of oxygen in the host liquid would increase the yield of the product or result. A higher concentration of the organism could be supported in the bioreactor, and when the rate of formation of the product is dependent on oxygen concentration, the rate will increase along with the increased levels of oxygen provided by the embodiments. In this application, the high level of oxygen would be adjusted to be below the level that results in excessive nucleation and formation of froth.


In anaerobic bioreactors, carbon monoxide may be used as a carbon source for biosynthesis of organic molecules. Applying the embodiments, high levels of carbon monoxide, including hyperbaric levels, are achievable in the host liquid, so that the reaction rate of the bioproduct can be accelerated. An increase in the reaction rate would make the process more efficient and more economical.


In the beverage industry, a high level of supersaturation of the beverage with a gas such as carbon dioxide is often desirable. The embodiments may be used to dispense a beverage highly supersaturated with a gas such as carbon dioxide, air, or oxygen. The gas-enriched liquid may be dispensed either as gas-enriched water that is mixed with ordinary syrup, or as the final gas-enriched beverage. Compared to the use of ordinary dispensers, the gas-enriched beverage provided by the embodiments will be less frothy and will retain the high level of gas for a longer period of time. Less froth will also expedite filling of a beverage glass or cup.


In the spa industry and in homes, the embodiments may be used to deliver water with a high level of gas supersaturation as provided in either a bath or a shower. The most economical gas is air, but air enriched with oxygen or pure oxygen can be used to provide high levels of oxygen in contact with the skin. High levels of oxygen may be helpful for enhancing collagen synthesis, reducing skin hypoxia, and oxidative killing of microorganisms. In addition, the fine effervescence that occurs in the water in contact with skin provides a unique invigorating sensation. In addition to air and oxygen, high levels of carbon dioxide in water can also be used for some applications, wherein vasodilation of skin vessels is desirable. A mixture of gases, such as carbon dioxide and oxygen, may also be beneficial in some instances.


There are numerous other examples, wherein a high level of gas in a host liquid under ambient pressure is achievable and advantageous with each embodiment. For example, water enriched with air can enhance water jet cleaning of surfaces and can facilitate snow making at temperatures above 0° C., and water enriched with an inert gas such as nitrogen or carbon dioxide can be used to more efficiently extinguish a fire.


The embodiments may be used with a wide variety of liquids. For example, liquid fuels, such as alcohols, oils, gasoline, and diesel fuel can be enriched with oxygen and, when delivered through a small orifice, subsequent combustion and oxidation of the fuel will be more complete. The presence of oxygen already in the fuel may act as a catalyst and/or the combustion may proceed at a higher temperature. In addition to the presence of oxygen in the fuel (the solubility of oxygen in fuels is much greater than for water), production of a fine mist from a small orifice can be used to produce microscopic bubbles suspended in a gaseous environment (e.g., air). The microbubbles are produced when the liquid first breaks up into tiny droplets and gas nucleation in each droplet produces a microbubble. The thin skin of fuel comprising the wall of the microbubble provides a very broad surface area for facilitating more complete combustion of the fuel. As a result, fuel efficiency will increase and emission of undesirable reactants, products, and particulate will be reduced.


It should be apparent that the embodiments may also be used to enhance any chemical or biologic reaction, wherein a high level of gas within a liquid is advantageous at ambient pressure. In addition to ordinary liquids, liquid melts of solids such as polymers and metals can be enriched with a gas with use of the embodiments.


The present invention may be susceptible to various modifications and alternative forms. Specific embodiments of the present invention are shown by way of example in the drawings and are described herein in detail. It should be understood, however, that the description set forth herein of specific embodiments is not intended to limit the present invention to the particular forms disclosed. Rather, all modifications, alternatives, and equivalents falling within the spirit and scope of the invention as defined by the appended claims are intended to be covered.

Claims
  • 1. A method of treating a wastewater comprising the acts of: pressurizing a vessel with a treatment gas; anddelivering the wastewater, in an atomized state, into the vessel to gas-enrich the wastewater to a desired gas content.
  • 2. The method of claim 1, comprising the acts of: withdrawing the wastewater from a supply of wastewater to be treated; andexpelling the wastewater, at about the desired gas content, back into the supply of wastewater.
  • 3. The method of claim 1, comprising the act of atomizing the wastewater.
  • 4. The method of claim 1, comprising the act of filtering the wastewater.
  • 5. The method of claim 4, wherein the act of filtering comprises passing the wastewater through a series of increasingly fine filters.
  • 6. The method of claim 4, wherein the act of filtering comprises passing the wastewater through a 150 to 450 micron filter.
  • 7. The method of claim 4, wherein the act of filtering the wastewater comprises passing the wastewater through a self cleaning filter.
  • 8. The method of claim 1, comprising the act of: delivering the wastewater to the vessel through a stinger disposed within the vessel, the stinger having a pipe adapted to carry the wastewater and at least one nozzle, operatively coupled to the pipe, to atomize the wastewater into the vessel.
  • 9. The method of claim 1, comprising the act of: delivering the wastewater to the vessel through at least one nozzle disposed adjacent to an inner wall of the vessel, the nozzle atomizing the wastewater into the vessel.
  • 10. A method of treating a wastewater, comprising the acts of: pressurizing a vessel with a treatment gas;delivering the wastewater, in an atomized state, into the vessel to gas-enrich the wastewater to a desired gas content;expelling the wastewater from the vessel through a fluid conduit; andpassing the wastewater through a nozzle coupled to the fluid conduit.
  • 11. The method of claim 10, wherein the act of expelling the wastewater comprises the act of passing the wastewater through a hose.
  • 12. The method of claim 10, wherein the act of passing the wastewater through the nozzle comprises the act of: passing the wastewater through a plurality of fluid passageways dimensioned to provide a substantially laminar and bubble-free flow.
  • 13. The method of claim 10, wherein the act of passing the wastewater through the nozzle comprises the act of: passing the wastewater through a plurality of stacked plates defining a plurality of fluid channels therebetween, the fluid channels having an inlet fluidically coupled to the fluid conduit and having an outlet.
  • 14. The apparatus of claim 10, wherein the act of passing the wastewater through the nozzle comprises the act of: passing the wastewater through a plurality of capillaries, each of the capillaries having an inlet fluidically coupled to the fluid conduit and having an outlet.
  • 15. A method of treating a wastewater, comprising the acts of: pressurizing a vessel with a treatment gas;delivering a water to be gas-enriched, in an atomized state, into the vessel to gas-enrich the water to a desired gas content;expelling the gas-enriched water from the vessel through a fluid conduit;delivering the gas-enriched water to a treatment site containing the wastewater to be treated; andadding the gas-enriched water to the wastewater,
  • 16. The method of claim 15, wherein the water to he gas-enriched is one selected from the consisting of: a tank of clean water, a pond, a lake, a stream, and a river.
  • 17. The method of claim 15, wherein the act of expelling the gas-enriched water is through a hose.
  • 18. The method of claim 15, further comprising the act of passing the gas-enriched water through a nozzle coupled to the fluid conduit.
  • 19. The method of claim 18, wherein the act of passing the gas-enriched water through the nozzle comprises the act of: passing the gas-enriched water through a plurality of stacked plates defining a plurality of fluid channels therebetween, the fluid channels having an inlet fluidically coupled to the fluid conduit and having an outlet.
  • 20. The method of claim 18, wherein the act of passing the gas-enriched water through the nozzle comprises the act of: passing the gas-enriched water through a plurality of capillaries, each of the capillaries having an inlet fluidically coupled to the fluid conduit and having an outlet.
CROSS-REFERENCE TO THE RELATED APPLICATION

This application is a divisional of U.S. patent application Ser. No. 09/632,530, filed Aug. 4, 2000, now U.S. Pat. No. 7,008,535.

US Referenced Citations (436)
Number Name Date Kind
604931 Eisendrath May 1898 A
1940341 Bansen et al. Dec 1933 A
2195273 Everson Mar 1940 A
2474665 Guarino Jun 1949 A
2700384 Ivory Jan 1955 A
2702035 Gibbon, Jr. et al. Feb 1955 A
2760922 Williams, Jr. Aug 1956 A
2827901 Jones Mar 1958 A
2847008 Taylor et al. Aug 1958 A
2876769 Cordova Mar 1959 A
2975606 Karwat Mar 1961 A
3037504 Everett Jun 1962 A
3097645 Lester Jul 1963 A
3133132 Loeb et al. May 1964 A
3142296 Love Jul 1964 A
3158150 Croasdaile et al. Nov 1964 A
3291463 Rousseau et al. Dec 1966 A
3295684 Webb Jan 1967 A
3300051 Mitchell Jan 1967 A
3406136 Scarso et al. Oct 1968 A
3437450 Greenwood Apr 1969 A
3456928 Selway Jul 1969 A
3459565 Jones et al. Aug 1969 A
3468136 Swenson et al. Sep 1969 A
3498286 Polanyi et al. Mar 1970 A
3512517 Kadish et al. May 1970 A
3584792 Johnson Jun 1971 A
3623474 Heilman et al. Nov 1971 A
3628758 Nichols Dec 1971 A
3648694 Mogos et al. Mar 1972 A
3661724 Strickler May 1972 A
3701345 Heilman et al. Oct 1972 A
3721231 Hubert Mar 1973 A
3731679 Wilhelmson et al. May 1973 A
3752145 Runnells et al. Aug 1973 A
3761065 Rich et al. Sep 1973 A
3795088 Esmond Mar 1974 A
3812843 Wootten et al. May 1974 A
3828767 Spiroff Aug 1974 A
3841308 Tate Oct 1974 A
3851646 Sarns Dec 1974 A
3862715 Remenyik Jan 1975 A
3881483 Sausse May 1975 A
3881990 Burton et al. May 1975 A
3898637 Wolstenholme Aug 1975 A
3911138 Clark, Jr. Oct 1975 A
3921622 Cole Nov 1975 A
3927981 Viannay et al. Dec 1975 A
3954921 Yoshida et al. May 1976 A
3956124 Fast et al. May 1976 A
3957585 Malick May 1976 A
3963503 Mackenzie Jun 1976 A
3966439 Vennos Jun 1976 A
3972721 Hammel et al. Aug 1976 A
3995444 Clark et al. Dec 1976 A
4003369 Heilman et al. Jan 1977 A
4008047 Petersen Feb 1977 A
4027045 Fedotkin et al. May 1977 A
4038430 Drake et al. Jul 1977 A
4039639 Kankel et al. Aug 1977 A
4041180 Wilson Aug 1977 A
4055498 Radnoti Oct 1977 A
4064047 Bernreiter et al. Dec 1977 A
4071443 Gorski et al. Jan 1978 A
4104074 Rostoker Aug 1978 A
4122858 Schiff Oct 1978 A
4155362 Jess May 1979 A
4175545 Termanini Nov 1979 A
4196726 Ronzi Apr 1980 A
4196730 Wilson Apr 1980 A
4205042 Lobdell et al. May 1980 A
4235095 Liebermann Nov 1980 A
4239729 Hasegawa et al. Dec 1980 A
4275020 DiGregorio et al. Jun 1981 A
4285977 Yezek et al. Aug 1981 A
4303432 Torobin Dec 1981 A
4304257 Webster Dec 1981 A
4312341 Zissimopoulos et al. Jan 1982 A
4313828 Brownlee Feb 1982 A
4317731 Roberts, Jr. et al. Mar 1982 A
4321691 Norton Mar 1982 A
4323420 Masnari et al. Apr 1982 A
4323983 Lee et al. Apr 1982 A
4332907 Vieli Jun 1982 A
4332908 Vieli Jun 1982 A
4344429 Gupton et al. Aug 1982 A
4347326 Iwami et al. Aug 1982 A
4349892 Suzuki et al. Sep 1982 A
4354502 Colley et al. Oct 1982 A
4362621 Dobna et al. Dec 1982 A
4366169 White Dec 1982 A
4368478 Koto Jan 1983 A
4372491 Fishgal Feb 1983 A
4375812 Vaseen et al. Mar 1983 A
4378797 Osterholm Apr 1983 A
4382288 Silverman May 1983 A
4385635 Ruiz May 1983 A
4393863 Osterholm Jul 1983 A
4401431 Arp Aug 1983 A
4406656 Hattler et al. Sep 1983 A
4423725 Baran et al. Jan 1984 A
4432069 Rose et al. Feb 1984 A
4436579 Rose et al. Mar 1984 A
4442843 Rasor et al. Apr 1984 A
4443480 Clark, Jr. Apr 1984 A
4445500 Osterholm May 1984 A
4445886 Osterholm May 1984 A
4445887 Osterholm May 1984 A
4445896 Gianturco May 1984 A
4448188 Loeb May 1984 A
4450841 Osterholm May 1984 A
4451251 Osterholm May 1984 A
4459977 Pizon et al. Jul 1984 A
4466804 Hino Aug 1984 A
4475666 Bilbrey et al. Oct 1984 A
4493692 Reed Jan 1985 A
4502129 Suzuki et al. Feb 1985 A
4509523 Pevsner Apr 1985 A
4531936 Gordon Jul 1985 A
4536293 Babineaux, III Aug 1985 A
4537387 Danby et al. Aug 1985 A
4538622 Samson et al. Sep 1985 A
4540399 Litzie et al. Sep 1985 A
4569836 Gordon Feb 1986 A
4572203 Feinstein Feb 1986 A
4573476 Ruiz Mar 1986 A
4576590 Fiddian-Green Mar 1986 A
4581012 Brown et al. Apr 1986 A
4582181 Samson Apr 1986 A
4596210 Schmidtke Jun 1986 A
4597412 Stark Jul 1986 A
4599462 Michl Jul 1986 A
4602987 Bonaventura et al. Jul 1986 A
4610661 Possis et al. Sep 1986 A
4619274 Morrison Oct 1986 A
4644808 Lecoffre Feb 1987 A
4645518 Roffelsen Feb 1987 A
4648384 Schmukler Mar 1987 A
4648865 Aigner Mar 1987 A
4657532 Osterholm Apr 1987 A
4657756 Rasor et al. Apr 1987 A
4658601 Burchell et al. Apr 1987 A
4661092 Popovich et al. Apr 1987 A
4661094 Simpson Apr 1987 A
4664680 Weber May 1987 A
4666668 Lidorenko et al. May 1987 A
4671287 Fiddian-Green Jun 1987 A
4674480 Lemelson Jun 1987 A
4674540 Takei et al. Jun 1987 A
4677100 Nakagawa et al. Jun 1987 A
4681119 Rasor et al. Jul 1987 A
4686085 Osterholm Aug 1987 A
4689149 Kanno et al. Aug 1987 A
4696195 Savonlahti et al. Sep 1987 A
4713344 Markhart, III Dec 1987 A
4715378 Pope, Jr. et al. Dec 1987 A
4721117 Mar et al. Jan 1988 A
4723939 Anaise Feb 1988 A
4729876 Hennessy et al. Mar 1988 A
4735750 Damann Apr 1988 A
4739768 Engelson Apr 1988 A
4739770 Stephens et al. Apr 1988 A
4748984 Patel Jun 1988 A
4748986 Morrison et al. Jun 1988 A
4758431 Osterholm Jul 1988 A
4761288 Mezei Aug 1988 A
4769241 Heldebrant et al. Sep 1988 A
4770168 Rusz et al. Sep 1988 A
4793350 Mar et al. Dec 1988 A
4800890 Cramer Jan 1989 A
4802650 Stricker Feb 1989 A
4804358 Karcher et al. Feb 1989 A
4808163 Laub Feb 1989 A
4808378 Nakanishi et al. Feb 1989 A
4815446 McIntosh Mar 1989 A
4827941 Taylor et al. May 1989 A
4828543 Weiss et al. May 1989 A
4830849 Osterholm May 1989 A
4834719 Arenas May 1989 A
4840617 Osterholm Jun 1989 A
4846193 Tremulis et al. Jul 1989 A
4850954 Charvin Jul 1989 A
4850958 Berry et al. Jul 1989 A
4865836 Long, Jr. Sep 1989 A
4869717 Adair Sep 1989 A
4871450 Goodrich et al. Oct 1989 A
4874509 Bullock Oct 1989 A
4874581 Sutherland et al. Oct 1989 A
4875489 Messner et al. Oct 1989 A
4877031 Conway et al. Oct 1989 A
4882097 Shannon Nov 1989 A
4884065 Crouse et al. Nov 1989 A
4919650 Feingold et al. Apr 1990 A
4919895 Heldebrant et al. Apr 1990 A
4921478 Solano et al. May 1990 A
4923442 Segall et al. May 1990 A
4927418 Dake et al. May 1990 A
4927623 Long, Jr. May 1990 A
4929317 Nishimura et al. May 1990 A
4930319 Bee et al. Jun 1990 A
4953553 Tremulis Sep 1990 A
4961731 Bodicky et al. Oct 1990 A
4963130 Osterholm Oct 1990 A
4964409 Tremulis Oct 1990 A
4965022 Litz Oct 1990 A
4966163 Kraus et al. Oct 1990 A
RE33451 Clark, Jr. Nov 1990 E
4968307 Dake et al. Nov 1990 A
4968483 Mūller et al. Nov 1990 A
4969878 Schmidt et al. Nov 1990 A
4973493 Guire Nov 1990 A
4973558 Wilson et al. Nov 1990 A
4979959 Guire Dec 1990 A
4981691 Osterholm et al. Jan 1991 A
4983747 Nishimura et al. Jan 1991 A
4985550 Charpiot et al. Jan 1991 A
4986809 Hattler Jan 1991 A
4991588 Pflueger et al. Feb 1991 A
5000739 Kulisz et al. Mar 1991 A
5002582 Guire et al. Mar 1991 A
5006110 Garrison et al. Apr 1991 A
5006352 Zelenák née Zoltai et al. Apr 1991 A
5009251 Pike et al. Apr 1991 A
5021044 Sharkawy Jun 1991 A
5029579 Trammell Jul 1991 A
5037403 Garcia Aug 1991 A
5039482 Panzani et al. Aug 1991 A
5044164 Bee Sep 1991 A
5050606 Tremulis Sep 1991 A
5055109 Gould et al. Oct 1991 A
5057120 Farcot Oct 1991 A
5059171 Bridge et al. Oct 1991 A
5059182 Laing Oct 1991 A
5059851 Corl et al. Oct 1991 A
5061236 Sutherland et al. Oct 1991 A
5061484 Heldebrant Oct 1991 A
5067489 Lind Nov 1991 A
5069661 Trudell Dec 1991 A
5072739 John Dec 1991 A
5080885 Long, Jr. Jan 1992 A
5084011 Grady Jan 1992 A
5086620 Spears Feb 1992 A
5087244 Wolinsky et al. Feb 1992 A
5098376 Berry et al. Mar 1992 A
5102390 Crittenden et al. Apr 1992 A
5104373 Davidner et al. Apr 1992 A
5106363 Nobuyoshi Apr 1992 A
5108662 Litz et al. Apr 1992 A
5110548 Montevecchi May 1992 A
5113013 Powell et al. May 1992 A
5114423 Kasprzyk et al. May 1992 A
5116317 Carson, Jr. et al. May 1992 A
5119807 Roberts Jun 1992 A
5124088 Stumphauzer Jun 1992 A
5135517 McCoy Aug 1992 A
5137513 McInnes et al. Aug 1992 A
5147311 Pickhard Sep 1992 A
5152964 Leonard Oct 1992 A
5158533 Strauss et al. Oct 1992 A
5158540 Wijay et al. Oct 1992 A
5158548 Lau et al. Oct 1992 A
5166573 Brown Nov 1992 A
5171216 Dasse et al. Dec 1992 A
5178603 Prince Jan 1993 A
5180364 Ginsburg Jan 1993 A
5181908 Bell Jan 1993 A
5184627 de Toledo Feb 1993 A
5186713 Raible Feb 1993 A
5195971 Sirhan Mar 1993 A
5199939 Dake et al. Apr 1993 A
5203338 Jang Apr 1993 A
5207869 Harmoning et al. May 1993 A
5209720 Unger May 1993 A
5211546 Isaacson et al. May 1993 A
5211627 William May 1993 A
5211636 Mische May 1993 A
5211637 Goto et al. May 1993 A
5213576 Abiuso et al. May 1993 A
5215680 D'Arrigo Jun 1993 A
5217492 Guire et al. Jun 1993 A
5218958 Cooper Jun 1993 A
5219099 Spence et al. Jun 1993 A
5219326 Hattler Jun 1993 A
5221483 Glenn et al. Jun 1993 A
5226888 Arney Jul 1993 A
5236416 McDaniel et al. Aug 1993 A
5240004 Walinsky et al. Aug 1993 A
5241985 Faust et al. Sep 1993 A
5252159 Arney Oct 1993 A
5254772 Dukat et al. Oct 1993 A
5261875 Spears Nov 1993 A
5271406 Ganguly et al. Dec 1993 A
5273052 Kraus et al. Dec 1993 A
5277176 Habashi et al. Jan 1994 A
5279562 Sirhan et al. Jan 1994 A
5279565 Klein et al. Jan 1994 A
5302168 Hess Apr 1994 A
5304325 Kaufman et al. Apr 1994 A
5308320 Safar et al. May 1994 A
5322500 Johnson et al. Jun 1994 A
5322508 Viera Jun 1994 A
5322511 Armbruster et al. Jun 1994 A
5324263 Kraus et al. Jun 1994 A
5324436 John et al. Jun 1994 A
5334142 Paradis Aug 1994 A
5339816 Akamatsu et al. Aug 1994 A
5341818 Abrams et al. Aug 1994 A
5342517 Kopf Aug 1994 A
5344393 Roth et al. Sep 1994 A
5344402 Crocker Sep 1994 A
5344930 Riess et al. Sep 1994 A
5356388 Sepetka et al. Oct 1994 A
5360396 Chan Nov 1994 A
5366696 Williams Nov 1994 A
5368555 Sussman et al. Nov 1994 A
5370640 Kolff Dec 1994 A
5372709 Hood Dec 1994 A
5374624 Segel Dec 1994 A
5376069 Hattler Dec 1994 A
5376083 Mische Dec 1994 A
5376240 Kaczur et al. Dec 1994 A
5380307 Chee et al. Jan 1995 A
5382407 Leonard Jan 1995 A
5383853 Jung et al. Jan 1995 A
5385821 O'Dell et al. Jan 1995 A
5393513 Long, Jr. Feb 1995 A
5394732 Johnson et al. Mar 1995 A
5395353 Scribner Mar 1995 A
5405329 Durand Apr 1995 A
5407424 LaFontaine et al. Apr 1995 A
5407425 Werner et al. Apr 1995 A
5407426 Spears Apr 1995 A
5409455 Belden Apr 1995 A
5409470 McIntyre et al. Apr 1995 A
5411466 Hess May 1995 A
5413558 Paradis May 1995 A
5417663 Slettenmark May 1995 A
5417969 Hsu et al. May 1995 A
5423741 Frank Jun 1995 A
5425703 Feiring Jun 1995 A
5433866 Hoppe et al. Jul 1995 A
5434191 Dandliker et al. Jul 1995 A
5437633 Manning Aug 1995 A
5438041 Zheng et al. Aug 1995 A
5439000 Gunderson et al. Aug 1995 A
5449342 Hirose et al. Sep 1995 A
5451211 Neer et al. Sep 1995 A
5456669 Neer et al. Oct 1995 A
5456670 Neer et al. Oct 1995 A
5462523 Samson et al. Oct 1995 A
5466216 Brown et al. Nov 1995 A
5480392 Mous Jan 1996 A
5487727 Snider et al. Jan 1996 A
5494576 Hoppe et al. Feb 1996 A
5498251 Dalton Mar 1996 A
5500096 Yuan Mar 1996 A
5507280 Henkin et al. Apr 1996 A
5509900 Kirkman Apr 1996 A
5527466 Li et al. Jun 1996 A
5527962 Pavia et al. Jun 1996 A
5533957 Aldea Jul 1996 A
5562608 Sekins et al. Oct 1996 A
5569180 Spears Oct 1996 A
5569197 Helmus et al. Oct 1996 A
5573668 Grosh et al. Nov 1996 A
5582574 Cramer Dec 1996 A
5589062 Rice Dec 1996 A
5591399 Goldman et al. Jan 1997 A
5599296 Spears Feb 1997 A
5605162 Mirzaee et al. Feb 1997 A
5612226 Williams Mar 1997 A
5620440 Heckele et al. Apr 1997 A
5621144 Cooper Apr 1997 A
5628755 Heller et al. May 1997 A
5634897 Dance et al. Jun 1997 A
5647976 Rothe et al. Jul 1997 A
5670094 Sasaki et al. Sep 1997 A
5693017 Spears et al. Dec 1997 A
5695473 Olsen Dec 1997 A
5695717 Polaschegg et al. Dec 1997 A
5702357 Bainbridge et al. Dec 1997 A
5702364 Euteneuer et al. Dec 1997 A
5702368 Stevens et al. Dec 1997 A
5706859 Bäcklund Jan 1998 A
5709654 Klatz et al. Jan 1998 A
5709658 Sirhan et al. Jan 1998 A
5716318 Manning Feb 1998 A
5720716 Blakeslee et al. Feb 1998 A
5725492 Igo et al. Mar 1998 A
5730330 Reading Mar 1998 A
5730698 Fischell et al. Mar 1998 A
5730935 Spears Mar 1998 A
5735934 Spears Apr 1998 A
5738644 Holmes et al. Apr 1998 A
5752929 Klatz et al. May 1998 A
5766490 Taylor et al. Jun 1998 A
5772624 Utterberg et al. Jun 1998 A
5786136 Mayer Jul 1998 A
5797874 Spears Aug 1998 A
5797876 Spears et al. Aug 1998 A
5798041 Zuk, Jr. Aug 1998 A
5798091 Trevino et al. Aug 1998 A
5799830 Carroll et al. Sep 1998 A
5800397 Wilson et al. Sep 1998 A
5807356 Finch, Jr. et al. Sep 1998 A
5810757 Sweezer, Jr. et al. Sep 1998 A
5810759 Merz Sep 1998 A
5814004 Tamari Sep 1998 A
5814125 Anderson et al. Sep 1998 A
5814222 Zelenák et al. Sep 1998 A
5817045 Sever, Jr. Oct 1998 A
5817046 Glickman Oct 1998 A
5820586 Booth et al. Oct 1998 A
5834519 Spears Nov 1998 A
5840067 Berguer et al. Nov 1998 A
5843023 Cecchi Dec 1998 A
5843307 Faivre et al. Dec 1998 A
5849005 Garrison et al. Dec 1998 A
5849191 Agranonik et al. Dec 1998 A
5849249 Jones, Jr. et al. Dec 1998 A
5869538 Van Liew et al. Feb 1999 A
5874093 Eliaz et al. Feb 1999 A
5879282 Fischell et al. Mar 1999 A
5882343 Wilson et al. Mar 1999 A
5885467 Zelenák et al. Mar 1999 A
5891111 Ismael Apr 1999 A
5893838 Daoud et al. Apr 1999 A
5916209 Mick Jun 1999 A
5922305 Spears Jul 1999 A
5935122 Fourkas et al. Aug 1999 A
5957899 Spears et al. Sep 1999 A
5957949 Leonhardt et al. Sep 1999 A
5958377 Spears Sep 1999 A
5976119 Spears et al. Nov 1999 A
5989210 Morris et al. Nov 1999 A
6398971 Butters et al. Jun 2002 B1
Foreign Referenced Citations (39)
Number Date Country
2 343 845 Mar 1974 DE
2649126 May 1978 DE
4105726 Sep 1992 DE
0 238 773 Mar 1986 EP
0 279 379 Aug 1988 EP
0 282 948 Sep 1988 EP
0 291 612 Nov 1988 EP
0 328 035 Feb 1989 EP
0 363 516 Apr 1990 EP
0 490 459 Jun 1992 EP
0 597 195 May 1994 EP
0 619 122 Oct 1994 EP
1.320.820 Feb 1963 FR
2 320 908 Nov 1977 FR
1 512 637 Jun 1978 GB
2 086 247 Jul 1981 GB
59-130812 Jul 1984 JP
59-130813 Jul 1984 JP
63-208523 Aug 1988 JP
901895 Jan 1982 RU
WO 9214404 Sep 1992 WO
WO 9214976 Sep 1992 WO
WO 9415659 Jul 1994 WO
WO 9513843 May 1995 WO
WO 9601593 Jan 1996 WO
WO 9617565 Jun 1996 WO
WO 9632157 Oct 1996 WO
WO 9640334 Dec 1996 WO
WO 9641987 Dec 1996 WO
WO 9711735 Apr 1997 WO
WO 9719713 Jun 1997 WO
WO 9749447 Dec 1997 WO
WO 9816203 Apr 1998 WO
WO 9846340 Oct 1998 WO
WO 9908732 Feb 1999 WO
WO 9908733 Feb 1999 WO
WO 9962584 Dec 1999 WO
WO 0004943 Feb 2000 WO
WO 9711870 Feb 2002 WO
Related Publications (1)
Number Date Country
20060054554 A1 Mar 2006 US
Divisions (1)
Number Date Country
Parent 09632530 Aug 2000 US
Child 11267795 US