Treating and sanitation of food, equipment, pharmaceutical products, and even water to reduce undesirable biological microorganisms is important to the protection of public health. For example, food can be damaged by microbes, spores, insects, and other similar sources. Each year, economic losses of food and labor due to damage from such sources is more than $100 billion. Currently, food items are preserved using a variety of methods, including refrigeration, fumigation with toxic chemicals, irradiation, biological control, heat exposure, and controlled atmosphere storage (a fruit industry technique that involves modifying the concentration of gases naturally present in the air).
The primary problem regarding food spoilage in public health is microbial growth. If pathogenic microorganisms are present, then growth can potentially lead to food-borne outbreaks and significant economic losses. Food safety concerns have been brought to the consumers' attention since the early part of the 20th century and those concerns have become even stronger today. Outbreaks from Salmonella and E. coli have increased the focus on food safety, including from a regulatory perspective. A study completed by the Centers for Disease Control and Prevention (CDC) estimated that food-borne diseases cause approximately 76 million illnesses, 325,000 hospitalizations, and 5,000 deaths annually in the US. Those numbers reveal the dramatic need for effective means of handling food products in order to ensure food safety.
Effective sanitation of food or other items depends on the combination of what is to be sanitized and the sanitation process type. Not all of the currently available technologies can deliver an effective reduction of microorganisms and at the same time prevent product or environmental degradation. It is well known in the art to cool products, such as foods, during processing with some type of refrigerant to slow down the growth of unwanted microbes and enzymatic reactions in foods. For instance, the shelf life and quality of food products are improved by processing, transporting, and storing under refrigerated conditions.
Cooling agents, such as water ice, dry ice, carbon dioxide, or nitrogen, are liquid or solid agents that can be used as an expendable refrigerant. In food processing applications, liquids, such as nitrogen, are used to cool and inert the atmosphere during food processing or storage.
While refrigeration can retard microbial growth, such treatment does not necessarily kill bacteria. Accordingly, microorganisms can still survive through refrigeration, and worse, some microorganisms can still grow and produce harmful substances during refrigerated storage. Furthermore, it is possible that the refrigerant used to cool a target item or food product can itself be contaminated with pathogenic microorganisms, thus contaminating the target item or food product.
Biocidal agents are used to sanitize equipment, provide antiseptic environments, treat water, and sanitize foods. The reaction of biocidal agents with microbial cell structures is often irreversible; therefore the cells either become attenuated or die.
One biocidal agent commonly used in the industry is ozone. However, ozone is very unstable, and therefore, must be produced at the location of consumption. Production of ozone requires specialized equipment and involves safety issues due to handling of the equipment and feedstock, such as pure oxygen. After the ozone is produced, it must be delivered in some form to the target item as a sanitizer. Ozone is often dissolved or absorbed in water as a mechanism to deliver the unstable ozone to a target item. However, ozone has poor solubility in water. Mixtures of ozone and water typically contain less than about 20 ppm by weight (ppmwt) ozone. As a result, large quantities of water relative to the ozone are required if water is used as a delivery agent. Furthermore, because of the large quantities of water required, the ozone and water cannot be pre-mixed and transported to site. Thus, ozone and water must be mixed on site.
Another problem with ozone is the difficulty in compressing an ozone-containing stream. There are no commercial processes known to one of ordinary skill in the art that are capable of delivering ozone at high pressures. Ozone generating equipment known in the art typically produces an ozone-containing gas stream at fairly low pressures. These ozone generators are typically limited to producing a stream with a pressure of less than about 25 psig. Conventional mechanical compression cannot be used to compress ozone because the unstable ozone molecule is destroyed in conventional compressors. Oil-lubricated or water ring compression can be used to compress a stream containing ozone up to 150 psig; however, these compressors inherently contaminate the ozone stream with oil or water respectively. Therefore, the prior art fails to provide a method to compress the ozone to pressures above about 25 psig without contaminating the ozone stream with some level of oil or water. Furthermore, the prior art fails to provide any method to successfully compress an ozone stream to pressures of greater than about 150 psig without destroying the ozone.
It is desirable to pressurize ozone to be used to sanitize equipment or devices and process foods. It is particularly desirable to be able to provide ozone in a pressurized stream at pressures above 150 psig without contaminating the ozone with oil or water. Further yet, it is desirable to pressurize ozone and feed it into a liquid, so that it is absorbed under pressure into the liquid and the liquid can them be used to treat of sanitize devices or food products.
The current invention fulfills the need to provide a process to pressurize an ozone-containing stream without destroying the ozone or contaminating the ozone-containing stream with oil or water. It is desirable to be able to provide a pressurized ozone-containing stream that is substantially free of oil and moisture. It is also desirable to the ozone-containing stream at pressures above 150 psig. It further desirable to pressurize ozone and feed it into a liquid, so that it is absorbed under pressure into the liquid.
The current invention pressurizes ozone by feeding an ozone-containing source to an ozone pressurization system to establish a first pressure followed by pressurizing the ozone pressurization system. The ozone pressurization system is pressurized by feeding a pressurization gas to the ozone pressurization system to raise the pressure to the second pressure and form a pressurized ozone-containing gas. The pressurized ozone-containing gas is then withdrawn from the ozone pressurization system. This method pressurizes the ozone-containing stream without contaminating the stream with oil or water.
In one embodiment, the ozone pressurization system comprises a pressurization vessel, the pressurization gas is fed into the lower portion of the pressurization vessel, and the pressurized ozone-containing gas is withdrawn from the upper portion of the pressurization vessel.
In another embodiment, the pressurization system comprises a first pressurization vessel and a last pressurization vessel. In this embodiment, the pressurization vessels are fluidly connected in series and the pressurizing gas is fed exclusively to the first pressurization vessel.
The current inventive method also provides a method to produce an ozonated liquid by feeding an ozone-containing gas from the ozone source to an ozone pressurization system to establish a first pressure, pressurizing the ozone pressurization system by feeding a pressurization gas into the system; thus, raising the pressure of the ozone-containing gas to a second pressure and forming a pressurized ozone-containing gas. This method also places a liquefied dry gas in an expansion vessel, and sparges the pressurized ozone-containing gas through the liquefied dry gas to form an ozonated liquefied dry gas, which is withdrawn from the expansion vessel.
For a further understanding of the nature and objects of the present invention, reference should be made to the following detailed description, taken in conjunction with the accompanying drawings, in which like elements are given the same or analogous reference numbers and wherein:
The current invention provides a method of pressurizing an ozone-containing stream without destroying the ozone or contaminating the ozone-containing stream with oil or water. Furthermore, the method forms an ozonated liquefied dry gas by bubbling the pressurized ozone-containing stream through a reservoir of liquefied dry gas.
The current invention pressurizes ozone by feeding an ozone-containing source to an ozone pressurization system to establish a first pressure followed by pressurizing the ozone pressurization system. The ozone pressurization system is pressurized by feeding a pressurization gas to the ozone pressurization system to raise the pressure to the second pressure and form a pressurized ozone-containing gas. The pressurized ozone-containing gas is then withdrawn from the ozone pressurization system.
In one preferred method, the pressurization gas is a dry gas. One preferred dry gas is CO2. The method pressurizes the ozone-containing stream without contaminating the stream with oil or water. The method preferable pressurizes the ozone-containing stream to a pressure that is greater than about 150 psig. Furthermore, the method can pressurize the ozone-containing stream from a pressure of less than about 50 psig to a pressure that is preferably greater than about 150 psig and even more preferably greater than about 200 psig.
In one embodiment of the method, the ozone pressurization system comprises a pressurization vessel, the pressurization gas is fed into the lower portion of the pressurization vessel, and the pressurized ozone-containing gas is withdrawn from the upper portion of the pressurization vessel.
In another embodiment, the pressurization system comprises a first pressurization vessel and a last pressurization vessel. In this embodiment, the pressurization vessels are fluidly connected in series and the pressurizing gas is fed exclusively to the first pressurization vessel. In a preferred embodiment, the pressurized gas mixture is withdrawn from the first pressurization vessel and fed to the last pressurization vessel, while the pressurized ozone-containing gas is withdrawn from the last pressurization vessel. In a further preferred embodiment, the pressurization gas is fed into a lower portion of the first pressurization vessel while the pressurized gas mixture is withdrawn from an upper portion of that first pressurization vessel. The pressurized gas mixture is then fed into a lower portion of the last pressurization vessel and the pressurized ozone-containing gas is finally withdrawn from an upper portion of the last pressurization vessel.
In yet a further embodiment, the pressurization system comprises a number of pressurization vessels in series and includes the steps of withdrawing a pressurized gas mixture from the first pressurization vessel, feeding the pressurized gas mixture to a successive pressurization vessel, and transferring the pressurized gas mixture from the successive pressurization vessel to the last pressurization vessel. This embodiment, like those above withdraws the pressurized ozone-containing gas from the last pressurization vessel. One further embodiment of this method feeds the pressurization gas into a lower portion of the first pressurization vessel, withdraws the pressurized gas is from an upper portion of the first pressurization vessel, feeds the pressurized gas mixture into a lower portion of the successive pressurization vessel, withdraws that pressurized gas from an upper portion of the successive pressurization vessel, and ultimately transfers the pressurized gas mixture into a lower portion of the last pressurization vessel.
The current inventive method also provides an ozonated liquid by feeding an ozone-containing gas from the ozone source to an ozone pressurization system to establish a first pressure, pressurizing the ozone pressurization system by feeding a pressurization gas into the system thus raising the pressure of the ozone-containing gas to a second pressure and forming a pressurized ozone-containing gas. The method also places a liquefied dry gas in an expansion vessel, and sparges the pressurized ozone-containing gas through the liquefied dry gas to form an ozonated liquefied dry gas, which is withdrawn from the expansion vessel. This method may further include steps of withdrawing a vent gas from the expansion tank and recycling the vent gas to a liquefied dry gas storage vessel. In some embodiments, the sparging occurs substantially continuously.
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One preferred pressurization gas 110 is a dry gas. The dry gas can be any suitable non-aqueous gas, but is preferably a liquefied gas, particularly a liquefied gas with a high gas density compared to the ozone-containing gas 102. The dry gas preferably contains less than 0.05 wt % water, and more preferably containing less than 20 ppm wt water. In one preferred embodiment, the pressurization gas 110 is preferably a dry gas that is stored as a liquid, such as CO2. The liquefied dry gas is removed from the liquid storage vessel and expanded to form the pressurization gas 110. One preferred embodiment uses a pressurization gas 110 that has a gas density that is higher that the gas density of the ozone-containing gas 102. This pressurization gas 110 is preferably cold after expansion to provide a pressurization gas at the highest gas density possible for that gas. In one embodiment, the pressurization gas is preferably less than about 20° C. after expansion, and more preferably less than about 10° C. after expansion. By using a pressurization gas 110 that is higher in gas density than the ozone-containing gas 102, and by feeding the pressurization gas 110 slowly, dilution of the ozone-containing gas 102 with the pressurization gas 110 is minimized. Without being limited by this theory, it is believed that the higher gas density pressurization gas 110 layers out in the pressurization vessel 112 below the lower density ozone-containing gas 102 already in the vessel. In one embodiment, the concentration of ozone in the pressurized ozone-containing gas 108 is at least about 70% of the concentration of ozone in the ozone-containing gas 102, more preferably at least 80% of the concentration of ozone in the ozone-containing gas 102, and even more preferably at least about 90% of the concentration of ozone in the ozone-containing gas 102.
In one embodiment, a continuous flow of pressurized ozone gas 110 is supplied by using a plurality of ozone pressurization systems 106 operated in a “round robin” to maximize the use of the ozone generator and minimize the waste of pressurization gas 110 by cross-tying (not shown) the sets of ozone pressurization systems 106.
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In one embodiment of the current invention, a continuous supply of pressurized ozone feed is supplied. In the embodiment, the pressurization vessels upstream of the last pressurization vessel 204 are replenished with ozone-containing gas 102. To accomplish this, the tanks upstream of the last pressurization vessel 204 are vented of their pressure, purged, re-filled with the ozone-containing gas 102, and re-pressurized as described above. This new batch of pressurized gas may then be released into the last pressurization vessel 204. This re-filling gives a slightly more dilute ozone mixture. A more efficient arrangement consists of several sets of tanks, operated in a “round robin” to maximize the use of the ozone generator, capture all pressurized ozone that does not reach the last pressurization vessel 204, and minimize the waste of pressurization gas 110 by allowing the sets of tanks to be cross-tied.
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Another embodiment of the dry gas pressurization method described above is used to dose other liquids, including aqueous and dry (non-aqueous) liquids. In one embodiment of the invention, the dry gas compression method is used to ozonate a liquid, where the liquid is at pressures greater than about 150 psig. In this embodiment, a liquid is placed into a pressure vessel where the pressure is greater than about 150 (or is raised to above this pressure), preferably great than about 200 psig, and more preferably greater than about 300 psig. The ozone pressurization system provides the pressurized ozone-containing gas at a second pressure, which is above the pressure in the pressure vessel, preferably at least about 50 psig above the pressure in the expansion vessel, and more preferably at least about 100 psig above the pressure in the expansion vessel. The ozonated liquid is withdrawn from the pressure vessel after sufficient sparging to assure the liquid contains a desired amount of ozone.
Although the present invention has been described in considerable detail with reference to certain preferred versions and examples thereof, other versions are possible. For instance, any liquid which one skilled in the art wishes to saturate with ozone can be substituted for the liquefied dry gas of the current invention in the method. Furthermore, there is a large variety of configurations of vessels, pipes, and other equipment that can be used as pressurization vessels. Clearly, the current invention may be used in a variety of processes for processing food, or non-food items. Therefore, the spirit and scope of the appended claims should not be limited to the description of the preferred versions contained herein.
All the features disclosed in this specification (including any accompanying claims, abstract, and drawings) may be replaced by alternative features serving the same, equivalent or similar purpose, unless expressly stated otherwise. Thus, unless expressly stated otherwise, each feature disclosed is one example only of a generic series of equivalent or similar features.
This application is a continuation-in-part of and claims priority to U.S. application Ser. No. 11/145,137, filed Jun. 3, 2005, entitled, “Novel Biological Treating Agent,” which is a continuation-in-part of and claims priority to U.S. application Ser. No. 10/632,232, filed Jul. 31, 2003, which is a non-provisional application claiming priority of U.S. Provisional application 60/404,635, filed Aug. 20, 2002, and U.S. Provisional application 60/459,398, filed Apr. 1, 2003. This application also claims priority to U.S. Provisional application 60/638,020, filed Dec. 21, 2004. The entire contents of these applications are hereby incorporated by reference.
Number | Date | Country | |
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60404635 | Aug 2002 | US | |
60459398 | Apr 2003 | US | |
60638020 | Dec 2004 | US |
Number | Date | Country | |
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Parent | 11145137 | Jun 2005 | US |
Child | 11281996 | Nov 2005 | US |
Parent | 10632232 | Jul 2003 | US |
Child | 11145137 | Jun 2005 | US |